Phentermine Hydrochloride PHENTERMINE HYDROCHLORIDE CHARTWELL RX, LLC FDA Approved Phentermine hydrochloride is a sympathomimetic amine anorectic. Its chemical name is α, α, -dimethylphenethylamine hydrochloride. The structural formula is as follows: Phentermine hydrochloride is a white, odorless, hygroscopic, crystalline powder which is soluble in water and lower alcohols, slightly soluble in chloroform and insoluble in ether. Each 8 mg contains Phentermine Hydrochloride, USP, and inactive ingredients include hydrogenated vegetable oil, lactose monohydrate, microcrystalline cellulose, colloidal silicon dioxide and magnesium stearate. "Image Description"
FunFoxMeds bottle
Route
ORAL
Applications
ANDA083923
Package NDC

Drug Facts

Composition & Profile

Quantities
90 tablets
Treats Conditions
Indications And Usage Phentermine Hydrochloride Tablets Are Indicated As A Short Term A Few Weeks Adjunct In A Regimen Of Weight Reduction Based On Exercise Behavioral Modification And Caloric Restriction In The Management Of Exogenous Obesity In Patients With An Initial Body Mass Index Greater Than Or Equal To 30 Kg M Or Greater Than Or Equal To 27 Kg M In The Presence Of Other Risk Factors E G Controlled Hypertension Diabetes Hyperlipidemia Below Is A Chart Of Body Mass Index Bmi Based On Various Heights And Weights Bmi Is Calculated By Taking The Patient S Weight In Kilograms Kg Divided By The Patient S Height In Meters M Squared Metric Conversions Are As Follows Pounds 2 2 Kg Inches X 0 0254 Meters Body Mass Index Bmi Kg M 2 The Limited Usefulness Of Agents Of This Class Including Phentermine See Clinical Pharmacology Should Be Measured Against Possible Risk Factors Inherent In Their Use Such As Those Described Below Image Description
Pill Appearance
Shape: round Color: white Imprint: C;E;263

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UPC
0362135959906
UNII
0K2I505OTV
Packaging

HOW SUPPLIED/STORAGE AND HANDLING Phentermine Hydrochloride Tablets, USP is supplied as white round scored tablets, debossed with " C " above the score line and " E " below on one side and " 263 " on the other side. Bottle of 90 tablets NDC 62135-959-90 Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight container as defined in the USP, with a child-resistant closure (as required). Keep out of the reach of children. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L72636 Rev. 08/2025; PRINCIPAL DISPLAY PANEL Phentermine Hydrochloride Tablets, USP CIV 8 mg - NDC 62135-959-90 - 90 Tabs Bottle Label "Image Description"

Package Descriptions
  • HOW SUPPLIED/STORAGE AND HANDLING Phentermine Hydrochloride Tablets, USP is supplied as white round scored tablets, debossed with " C " above the score line and " E " below on one side and " 263 " on the other side. Bottle of 90 tablets NDC 62135-959-90 Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight container as defined in the USP, with a child-resistant closure (as required). Keep out of the reach of children. Manufactured for: Chartwell RX, LLC. Congers, NY 10920 L72636 Rev. 08/2025
  • PRINCIPAL DISPLAY PANEL Phentermine Hydrochloride Tablets, USP CIV 8 mg - NDC 62135-959-90 - 90 Tabs Bottle Label "Image Description"

Overview

Phentermine hydrochloride is a sympathomimetic amine anorectic. Its chemical name is α, α, -dimethylphenethylamine hydrochloride. The structural formula is as follows: Phentermine hydrochloride is a white, odorless, hygroscopic, crystalline powder which is soluble in water and lower alcohols, slightly soluble in chloroform and insoluble in ether. Each 8 mg contains Phentermine Hydrochloride, USP, and inactive ingredients include hydrogenated vegetable oil, lactose monohydrate, microcrystalline cellulose, colloidal silicon dioxide and magnesium stearate. "Image Description"

Indications & Usage

Phentermine hydrochloride tablets are indicated as a short-term (a few weeks) adjunct in a regimen of weight reduction based on exercise, behavioral modification and caloric restriction in the management of exogenous obesity in patients with an initial body mass index greater than or equal to 30 kg/m , or greater than or equal to 27 kg/m in the presence of other risk factors (e.g., controlled hypertension, diabetes, hyperlipidemia). Below is a chart of body mass index (BMI) based on various heights and weights. BMI is calculated by taking the patient’s weight, in kilograms (kg), divided by the patient’s height, in meters (m), squared. Metric conversions are as follows: pounds ÷ 2.2 = kg; inches x 0.0254 = meters. BODY MASS INDEX (BMI), kg/m 2 The limited usefulness of agents of this class, including phentermine (see Clinical Pharmacology ), should be measured against possible risk factors inherent in their use such as those described below. "Image Description"

Dosage & Administration

Dosage should be individualized to obtain an adequate response with the lowest effective dose. The usual adult dose is one tablet three times a day ½ hour before meals. This tablet is scored to facilitate administering one half of the usual dosage for patients not requiring the full dose. Phentermine hydrochloride is not recommended for use in pediatric patients less than or equal to 16 years of age. Late evening medication should be avoided because of the possibility of resulting insomnia.

Warnings & Precautions
WARNINGS Coadministration with Other Drug Products for Weight Loss Phentermine hydrochloride tablets are indicated only as short-term (a few weeks) monotherapy for the management of exogenous obesity. The safety and efficacy of combination therapy with phentermine and any other drug products for weight loss including prescribed drugs, over-the-counter preparations, and herbal products, or serotonergic agents such as selective serotonin reuptake inhibitors (e.g., fluoxetine, sertraline, fluvoxamine, paroxetine), have not been established. Therefore, coadministration of phentermine and these drug products is not recommended. Primary Pulmonary Hypertension Primary Pulmonary Hypertension (PPH) – a rare, frequently fatal disease of the lungs – has been reported to occur in patients receiving a combination of phentermine with fenfluramine or dexfenfluramine. The possibility of an association between PPH and the use of phentermine alone cannot be ruled out; there have been rare cases of PPH in patients who reportedly have taken phentermine alone. The initial symptom of PPH is usually dyspnea. Other initial symptoms may include angina pectoris, syncope or lower extremity edema. Patients should be advised to report immediately any deterioration in exercise tolerance. Treatment should be discontinued in patients who develop new, unexplained symptoms of dyspnea, angina pectoris, syncope or lower extremity edema, and patients should be evaluated for the possible presence of pulmonary hypertension. Valvular Heart Disease Serious regurgitant cardiac valvular disease, primarily affecting the mitral, aortic and/or tricuspid valves, has been reported in otherwise healthy persons who had taken a combination of phentermine with fenfluramine or dexfenfluramine for weight loss. The possible role of phentermine in the etiology of these valvulopathies has not been established and their course in individuals after the drugs are stopped is not known. The possibility of an association between valvular heart disease and the use of phentermine alone cannot be ruled out; there have been rare cases of valvular heart disease in patients who reportedly have taken phentermine alone. Development of Tolerance, Discontinuation in Case of Tolerance When tolerance to the anorectant effect develops, the recommended dose should not be exceeded in an attempt to increase the effect; rather, the drug should be discontinued. Effect on the Ability to Engage in Potentially Hazardous Tasks Phentermine may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or driving a motor vehicle; the patient should therefore be cautioned accordingly. Risk of Abuse and Dependence Phentermine is related chemically and pharmacologically to amphetamine (d- and d/l-amphetamine) and other related stimulant drugs have been extensively abused. The possibility of abuse of phentermine should be kept in mind when evaluating the desirability of including a drug as part of a weight reduction program. See Adverse Reactions / Drug Abuse and Dependence and Overdosage . The least amount feasible should be prescribed or dispensed at one time in order to minimize the possibility of overdosage. Usage with Alcohol Concomitant use of alcohol with phentermine may result in an adverse drug reaction. Use in Patients with Hypertension Use caution in prescribing phentermine for patients with even mild hypertension (risk of increase in blood pressure). Use in Patients on Insulin or Oral Hypoglycemic Medications for Diabetes Mellitus A reduction in insulin or oral hypoglycemic medications in patients with diabetes mellitus may be required.
Contraindications

History of cardiovascular disease (e.g., coronary artery disease, stroke, arrhythmias, congestive heart failure, uncontrolled hypertension) During or within 14 days following the administration of monoamine oxidase inhibitors Hyperthyroidism Glaucoma Agitated states History of drug abuse Pregnancy (see Precautions ) Nursing (see Precautions ) Known hypersensitivity, or idiosyncrasy to the sympathomimetic amines

Adverse Reactions

The following adverse reactions are described, or described in greater detail, in other sections: Primary pulmonary hypertension (see Warnings ) Valvular heart disease (see Warnings ) Effect on the ability to engage in potentially hazardous tasks (see Warnings ) Withdrawal effects following prolonged high dosage administration (see Drug Abuse and Dependence ) The following adverse reactions to phentermine have been identified: Cardiovascular Primary pulmonary hypertension and/or regurgitant cardiac valvular disease, palpitation, tachycardia, elevation of blood pressure, ischemic events. Central Nervous System Overstimulation, restlessness, dizziness, insomnia, euphoria, dysphoria, tremor, headache, psychosis. Gastrointestinal Dryness of the mouth, unpleasant taste, diarrhea, constipation, other gastrointestinal disturbances. Allergic Urticaria. Endocrine Impotence, changes in libido.


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