Tigan 

(See WARNINGS and PRECAUTIONS.)

Dosage should be adjusted according to the indication for therapy, severity of symptoms and the response of the patient.

Geriatric Patients

Dose adjustment such as reducing the total dose administered at each dosing or increasing the dosing interval should be considered

in elderly patients with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m²). Final dose adjustment should be based upon

integration of clinical efficacy and safety considerations. (See CLINICAL PHARMACOLOGY and PRECAUTIONS).

Patients with Renal Impairment

In subjects with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m²), dose adjustment such as reducing the total dose

administered at each dosing or increasing the dosing interval should be considered. (See CLINICAL PHARMACOLOGY and

DOSAGE AND ADMINISTRATION).

INJECTABLE, 100 mg/mL (Not for use in pediatric patients)

    Usual Adult Dosage

    2 mL (200 mg) t.i.d. or q.i.d. intramuscularly.

NOTE: The injectable form is intended for intramuscular administration only; it is not recommended for intravenous use.

Intramuscular administration may cause pain, stinging, burning, redness and swelling at the site of injection. Such effects may be

minimized by deep injection into the upper outer quadrant of the gluteal region, and by avoiding the escape of solution along the route.

The injectable form of Tigan^® is contraindicated in pediatric patients and in patients with known hypersensitivity to

trimethobenzamide.

There have been reports of hypersensitivity reactions and Parkinson-like symptoms. There have been instances of hypotension

reported following parenteral administration to surgical patients. There have been reports of blood dyscrasias, blurring of vision,

coma, convulsions, depression of mood, diarrhea, disorientation, dizziness, drowsiness, headache, jaundice, muscle cramps

and opisthotonos. If these occur, the administration of the drug should be discontinued. Allergic-type skin reactions have been

observed; therefore, the drug should be discontinued at the first sign of sensitization. While these symptoms will usually disappear

spontaneously, symptomatic treatment may be indicated in some cases.

For medical advice about adverse reactions contact your medical professional. To report SUSPECTED ADVERSE REACTIONS,

contact Endo at 1-800-828-9393 or FDA at 1-800-FDA-1088 (1-800-332-1088) or www.fda.gov/medwatch.

Tigan^® (trimethobenzamide hydrochloride) is available as follows:

NDC 42023-119-25 100 mg/mL in 2 mL Single-Dose Vials,

Pack of 25

Rx Only

Manufactured for:

Endo USA

Malvern, PA 19355

© 2025 Endo, Inc. or one of its affiliates.

R08/2024

OS118J-01-90-04

3000358J

Chemically, trimethobenzamide (HCl) is N-[p-[2-(dimethylamino)ethoxy]benzyl]-3,4,5-trimethoxybenzamide monohydrochloride. It

has a molecular weight of 424.93 and the following structural formula:

Single Dose Vials: Each 2-mL single-dose vial contains 200 mg trimethobenzamide hydrochloride compounded with 1 mg sodium citrate and 0.4 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

Multi-Dose Vials: Each mL contains 100 mg trimethobenzamide hydrochloride compounded with 0.45% phenol as preservative, 0.5 mg sodium citrate and 0.2 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

For Intramuscular Use Only

Not for Use in Pediatric Patients

Store between 20° to 25°C (68° to 77°F).

(See USP Controlled Room Temperature.)

Tigan ^® may produce drowsiness. Patients should not operate motor vehicles or other dangerous machinery until their individual

responses have been determined.

Usage in Pregnancy:

Trimethobenzamide hydrochloride was studied in reproduction experiments in rats and rabbits and no teratogenicity was suggested.

The only effects observed were an increased percentage of embryonic resorptions or stillborn pups in rats administered 20 mg and

100 mg/kg and increased resorptions in rabbits receiving 100 mg/kg. In each study these adverse effects were attributed to one or

two dams. The relevance to humans is not known. Since there is no adequate experience in pregnant or lactating women who have

received this drug, safety in pregnancy or in nursing mothers has not been established.

Usage with Alcohol:

Concomitant use of alcohol with Tigan ^® may result in an adverse drug interaction.

Tigan ^® is indicated for the treatment of postoperative nausea and vomiting and for nausea associated with gastroenteritis.

During the course of acute febrile illness, encephalitides, gastroenteritis, dehydration and electrolyte imbalance, especially in

children and the elderly or debilitated, CNS reactions such as opisthotonos, convulsions, coma and extrapyramidal symptoms have

been reported with and without use of Tigan ^® (trimethobenzamide hydrochloride) or other antiemetic agents. In such disorders

caution should be exercised in administering Tigan ^®, particularly to patients who have recently received other CNS-acting agents

(phenothiazines, barbiturates, belladonna derivatives). Primary emphasis should be directed toward the restoration of body fluids and

electrolyte balance, the relief of fever and relief of the causative disease process. Overhydration should be avoided since it may result

in cerebral edema.

The antiemetic effects of Tigan ^® may render diagnosis more difficult in such conditions as appendicitis and obscure signs of toxicity

due to overdosage of other drugs.

General

Adjustment of Dose in Renal Failure

A substantial route of elimination of unchanged trimethobenzamide is via the kidney. Dosage adjustment should be considered in

patients with reduced renal function including some elderly patients. (See CLINICAL PHARMACOLOGY and DOSAGE AND

ADMINISTRATION).

Geriatric Use

Clinical studies of trimethobenzamide hydrochloride did not include sufficient numbers of patients aged 65 and over to determine

whether they respond differently from younger patients. Although there are studies reported in the literature that included elderly

patients > 65 years old with younger patients, it is not known if there are differences in efficacy or safety parameters for elderly and

non-elderly patients treated with trimethobenzamide. In general, dose selection for an elderly patient should be cautious, usually

starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of

concomitant disease or other drug therapy.

This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients

with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in

dose selection, and it may be useful to monitor renal function. (See CLINICAL PHARMACOLOGY and DOSAGE AND

ADMINISTRATION).

Mechanism of Action

The mechanism of action of Tigan^® as determined in animals is obscure, but may involve the chemoreceptor trigger zone (CTZ), an

area in the medulla oblongata through which emetic impulses are conveyed to the vomiting center; direct impulses to the vomiting

center apparently are not similarly inhibited. In dogs pretreated with trimethobenzamide HCl, the emetic response to apomorphine is

inhibited, while little or no protection is afforded against emesis induced by intragastric copper sulfate.

Pharmacokinetics

The pharmacokinetics of trimethobenzamide have been studied in healthy adult subjects. Following administration of 200 mg

(100 mg/mL) Tigan IM injection, the time to reach maximum plasma concentration (T_max) was about half an hour, about 15

minutes longer for Tigan 300 mg oral capsule than an I.M. injection. A single dose of Tigan 300 mg oral capsule provided a plasma

concentration profile of trimethobenzamide similar to Tigan 200 mg I.M. The relative bioavailability of the capsule formulation

compared to the solution is 100%. The mean elimination half-life of trimethobenzamide is 7 to 9 hours. Between 30 – 50% of a single

dose in humans is excreted unchanged in the urine within 48 – 72 hours. The metabolic disposition of trimethobenzamide in humans is

not known. Specifically, it is not known if active metabolites are generated in humans.

Special Populations

Age

The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider

reduction in the dosing of trimethobenzamide in elderly patients with renal impairment considering that a substantial amount of

excretion and elimination of trimethobenzamide occurs via the kidney and that elderly patients may have various degrees of renal

impairment. (See PRECAUTIONS: General and DOSAGE AND ADMINISTRATION).

Gender

Systemic exposure to trimethobenzamide was similar between men (N=40) and women (N=28).

Race

Pharmacokinetics appeared to be similar for Caucasians (N=53) and African Americans (N=12).

Renal Impairment

The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider

reduction in the dosing of trimethobenzamide in patients with renal impairment considering that a substantial amount of

excretion and elimination of trimethobenzamide occurs via the kidney. (See PRECAUTIONS: General and DOSAGE AND

ADMINISTRATION).

For Intramuscular Use Only

Not for Use in Pediatric Patients

Store between 20° to 25°C (68° to 77°F).

(See USP Controlled Room Temperature.)

Tigan ^® may produce drowsiness. Patients should not operate motor vehicles or other dangerous machinery until their individual

responses have been determined.

Usage in Pregnancy:

Trimethobenzamide hydrochloride was studied in reproduction experiments in rats and rabbits and no teratogenicity was suggested.

The only effects observed were an increased percentage of embryonic resorptions or stillborn pups in rats administered 20 mg and

100 mg/kg and increased resorptions in rabbits receiving 100 mg/kg. In each study these adverse effects were attributed to one or

two dams. The relevance to humans is not known. Since there is no adequate experience in pregnant or lactating women who have

received this drug, safety in pregnancy or in nursing mothers has not been established.

Usage with Alcohol:

Concomitant use of alcohol with Tigan ^® may result in an adverse drug interaction.

Chemically, trimethobenzamide (HCl) is N-[p-[2-(dimethylamino)ethoxy]benzyl]-3,4,5-trimethoxybenzamide monohydrochloride. It

has a molecular weight of 424.93 and the following structural formula:

Single Dose Vials: Each 2-mL single-dose vial contains 200 mg trimethobenzamide hydrochloride compounded with 1 mg sodium citrate and 0.4 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

Multi-Dose Vials: Each mL contains 100 mg trimethobenzamide hydrochloride compounded with 0.45% phenol as preservative, 0.5 mg sodium citrate and 0.2 mg citric acid as buffers and pH adjusted to approximately 5.0 with sodium hydroxide.

Tigan ^® is indicated for the treatment of postoperative nausea and vomiting and for nausea associated with gastroenteritis.

During the course of acute febrile illness, encephalitides, gastroenteritis, dehydration and electrolyte imbalance, especially in

children and the elderly or debilitated, CNS reactions such as opisthotonos, convulsions, coma and extrapyramidal symptoms have

been reported with and without use of Tigan ^® (trimethobenzamide hydrochloride) or other antiemetic agents. In such disorders

caution should be exercised in administering Tigan ^®, particularly to patients who have recently received other CNS-acting agents

(phenothiazines, barbiturates, belladonna derivatives). Primary emphasis should be directed toward the restoration of body fluids and

electrolyte balance, the relief of fever and relief of the causative disease process. Overhydration should be avoided since it may result

in cerebral edema.

The antiemetic effects of Tigan ^® may render diagnosis more difficult in such conditions as appendicitis and obscure signs of toxicity

due to overdosage of other drugs.

General

Adjustment of Dose in Renal Failure

A substantial route of elimination of unchanged trimethobenzamide is via the kidney. Dosage adjustment should be considered in

patients with reduced renal function including some elderly patients. (See CLINICAL PHARMACOLOGY and DOSAGE AND

ADMINISTRATION).

Geriatric Use

Clinical studies of trimethobenzamide hydrochloride did not include sufficient numbers of patients aged 65 and over to determine

whether they respond differently from younger patients. Although there are studies reported in the literature that included elderly

patients > 65 years old with younger patients, it is not known if there are differences in efficacy or safety parameters for elderly and

non-elderly patients treated with trimethobenzamide. In general, dose selection for an elderly patient should be cautious, usually

starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of

concomitant disease or other drug therapy.

This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients

with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in

dose selection, and it may be useful to monitor renal function. (See CLINICAL PHARMACOLOGY and DOSAGE AND

ADMINISTRATION).

Tigan^® (trimethobenzamide hydrochloride) is available as follows:

NDC 42023-119-25 100 mg/mL in 2 mL Single-Dose Vials,

Pack of 25

Rx Only

Manufactured for:

Endo USA

Malvern, PA 19355

© 2025 Endo, Inc. or one of its affiliates.

R08/2024

OS118J-01-90-04

3000358J

There have been reports of hypersensitivity reactions and Parkinson-like symptoms. There have been instances of hypotension

reported following parenteral administration to surgical patients. There have been reports of blood dyscrasias, blurring of vision,

coma, convulsions, depression of mood, diarrhea, disorientation, dizziness, drowsiness, headache, jaundice, muscle cramps

and opisthotonos. If these occur, the administration of the drug should be discontinued. Allergic-type skin reactions have been

observed; therefore, the drug should be discontinued at the first sign of sensitization. While these symptoms will usually disappear

spontaneously, symptomatic treatment may be indicated in some cases.

For medical advice about adverse reactions contact your medical professional. To report SUSPECTED ADVERSE REACTIONS,

contact Endo at 1-800-828-9393 or FDA at 1-800-FDA-1088 (1-800-332-1088) or www.fda.gov/medwatch.

The injectable form of Tigan^® is contraindicated in pediatric patients and in patients with known hypersensitivity to

trimethobenzamide.

Mechanism of Action

The mechanism of action of Tigan^® as determined in animals is obscure, but may involve the chemoreceptor trigger zone (CTZ), an

area in the medulla oblongata through which emetic impulses are conveyed to the vomiting center; direct impulses to the vomiting

center apparently are not similarly inhibited. In dogs pretreated with trimethobenzamide HCl, the emetic response to apomorphine is

inhibited, while little or no protection is afforded against emesis induced by intragastric copper sulfate.

Pharmacokinetics

The pharmacokinetics of trimethobenzamide have been studied in healthy adult subjects. Following administration of 200 mg

(100 mg/mL) Tigan IM injection, the time to reach maximum plasma concentration (T_max) was about half an hour, about 15

minutes longer for Tigan 300 mg oral capsule than an I.M. injection. A single dose of Tigan 300 mg oral capsule provided a plasma

concentration profile of trimethobenzamide similar to Tigan 200 mg I.M. The relative bioavailability of the capsule formulation

compared to the solution is 100%. The mean elimination half-life of trimethobenzamide is 7 to 9 hours. Between 30 – 50% of a single

dose in humans is excreted unchanged in the urine within 48 – 72 hours. The metabolic disposition of trimethobenzamide in humans is

not known. Specifically, it is not known if active metabolites are generated in humans.

Special Populations

Age

The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider

reduction in the dosing of trimethobenzamide in elderly patients with renal impairment considering that a substantial amount of

excretion and elimination of trimethobenzamide occurs via the kidney and that elderly patients may have various degrees of renal

impairment. (See PRECAUTIONS: General and DOSAGE AND ADMINISTRATION).

Gender

Systemic exposure to trimethobenzamide was similar between men (N=40) and women (N=28).

Race

Pharmacokinetics appeared to be similar for Caucasians (N=53) and African Americans (N=12).

Renal Impairment

The clearance of trimethobenzamide is not known in patients with renal impairment. However, it may be advisable to consider

reduction in the dosing of trimethobenzamide in patients with renal impairment considering that a substantial amount of

excretion and elimination of trimethobenzamide occurs via the kidney. (See PRECAUTIONS: General and DOSAGE AND

ADMINISTRATION).

(See WARNINGS and PRECAUTIONS.)

Dosage should be adjusted according to the indication for therapy, severity of symptoms and the response of the patient.

Geriatric Patients

Dose adjustment such as reducing the total dose administered at each dosing or increasing the dosing interval should be considered

in elderly patients with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m²). Final dose adjustment should be based upon

integration of clinical efficacy and safety considerations. (See CLINICAL PHARMACOLOGY and PRECAUTIONS).

Patients with Renal Impairment

In subjects with renal impairment (creatinine clearance ≤ 70 mL/min/1.73m²), dose adjustment such as reducing the total dose

administered at each dosing or increasing the dosing interval should be considered. (See CLINICAL PHARMACOLOGY and

DOSAGE AND ADMINISTRATION).

INJECTABLE, 100 mg/mL (Not for use in pediatric patients)

    Usual Adult Dosage

    2 mL (200 mg) t.i.d. or q.i.d. intramuscularly.

NOTE: The injectable form is intended for intramuscular administration only; it is not recommended for intravenous use.

Intramuscular administration may cause pain, stinging, burning, redness and swelling at the site of injection. Such effects may be

minimized by deep injection into the upper outer quadrant of the gluteal region, and by avoiding the escape of solution along the route.