Drug Facts
Composition & Profile
Identifiers & Packaging
16 HOW SUPPLIED/STORAGE AND HANDLING Vasopressin in Sodium Chloride Injection is a clear, colorless solution for intravenous administration available as: NDC 81298-8552-3: A carton of 10 single dose vials. Each vial contains vasopressin 20 units/100 mL (0.2 units/mL). NDC 81298-8554-3: A carton of 10 single dose vials. Each vial contains vasopressin 40 units/100 mL (0.4 units/mL). NDC 81298-8550-3: A carton of 10 single dose vials. Each vial contains vasopressin 50 units/50 mL (1 unit/mL). Store unopened vials refrigerated at 2°C to 8°C (36°F to 46°F). Do not freeze. Keep vials in original carton to protect from light. Vials may be held up to three (3) months upon removal from refrigeration to room temperature storage conditions (20°C to 25°C [68°F to 77°F], USP Controlled Room Temperature), anytime within the labeled shelf life. Once removed from refrigeration, unopened vial should be marked to indicate the revised three (3) months expiration date. If the manufacturer's original expiration date is shorter than the revised expiration date, then the shorter date must be used. Do not use Vasopressin in Sodium Chloride Injection beyond the manufacturer's expiration date stamped on the vial. Manufactured for: Long Grove Pharmaceuticals, LLC Rosemont, IL 60018 Made in India; Principal Display Panel – 20 Units per 100 mL Carton Label Vasopressin in 0.9% Sodium Chloride Injection 20 Units per 100 mL (0.2 units per mL) For intravenous infusion Ready to use 10 x 100 mL Single-Dose Vials Discard Unused Portion NDC 81298-8552-3 Rx only Recommended Dosage: See Prescribing Information. LONG GROVE™ PHARMACEUTICALS Principal Display Panel – 20 Units per 100 mL Carton Label; Principal Display Panel – 40 Units per 100 mL Carton Label Vasopressin in 0.9% Sodium Chloride Injection 40 Units per 100 mL (0.4 units per mL) For intravenous infusion Ready to use 10 x 100 mL Single-Dose Vials Discard Unused Portion NDC 81298-8554-3 Rx only Recommended Dosage: See Prescribing Information. LONG GROVE™ PHARMACEUTICALS Principal Display Panel – 40 Units per 100 mL Carton Label
- 16 HOW SUPPLIED/STORAGE AND HANDLING Vasopressin in Sodium Chloride Injection is a clear, colorless solution for intravenous administration available as: NDC 81298-8552-3: A carton of 10 single dose vials. Each vial contains vasopressin 20 units/100 mL (0.2 units/mL). NDC 81298-8554-3: A carton of 10 single dose vials. Each vial contains vasopressin 40 units/100 mL (0.4 units/mL). NDC 81298-8550-3: A carton of 10 single dose vials. Each vial contains vasopressin 50 units/50 mL (1 unit/mL). Store unopened vials refrigerated at 2°C to 8°C (36°F to 46°F). Do not freeze. Keep vials in original carton to protect from light. Vials may be held up to three (3) months upon removal from refrigeration to room temperature storage conditions (20°C to 25°C [68°F to 77°F], USP Controlled Room Temperature), anytime within the labeled shelf life. Once removed from refrigeration, unopened vial should be marked to indicate the revised three (3) months expiration date. If the manufacturer's original expiration date is shorter than the revised expiration date, then the shorter date must be used. Do not use Vasopressin in Sodium Chloride Injection beyond the manufacturer's expiration date stamped on the vial. Manufactured for: Long Grove Pharmaceuticals, LLC Rosemont, IL 60018 Made in India
- Principal Display Panel – 20 Units per 100 mL Carton Label Vasopressin in 0.9% Sodium Chloride Injection 20 Units per 100 mL (0.2 units per mL) For intravenous infusion Ready to use 10 x 100 mL Single-Dose Vials Discard Unused Portion NDC 81298-8552-3 Rx only Recommended Dosage: See Prescribing Information. LONG GROVE™ PHARMACEUTICALS Principal Display Panel – 20 Units per 100 mL Carton Label
- Principal Display Panel – 40 Units per 100 mL Carton Label Vasopressin in 0.9% Sodium Chloride Injection 40 Units per 100 mL (0.4 units per mL) For intravenous infusion Ready to use 10 x 100 mL Single-Dose Vials Discard Unused Portion NDC 81298-8554-3 Rx only Recommended Dosage: See Prescribing Information. LONG GROVE™ PHARMACEUTICALS Principal Display Panel – 40 Units per 100 mL Carton Label
Overview
Vasopressin is a polypeptide hormone. Vasopressin in Sodium Chloride Injection is a sterile, aqueous solution of synthetic arginine vasopressin for intravenous administration. Each mL of the 0.2 unit/mL strength contains 0.2 units vasopressin, 0.0672 mg aspartic acid, 0.0180 mg boric acid, 0.05 mg chlorobutanol, 9 mg sodium chloride and Water for Injection, USP. Each mL of the 0.4 unit/mL strength contains 0.4 units vasopressin, 0.0672 mg aspartic acid, 0.0180 mg boric acid, 0.10 mg chlorobutanol, 9 mg sodium chloride and Water for Injection, USP. Each mL of the 1 unit/mL strength contains 1 unit vasopressin, 0.0672 mg aspartic acid, 0.0180 mg boric acid, 0.25 mg chlorobutanol, 9 mg sodium chloride and Water for Injection, USP. The chemical name of vasopressin is Cyclo (1-6) L-Cysteinyl-L-Tyrosyl-L-Phenylalanyl-L-Glutaminyl- L-Asparaginyl-L-Cysteinyl-L-Prolyl-L-Arginyl-L-Glycinamide. It is a white to off-white amorphous powder, freely soluble in water. The structural formula is: Molecular Formula: C 46 H 65 N 15 O 12 S 2 Molecular Weight: 1084.23 Structural Formula
Indications & Usage
Vasopressin in Sodium Chloride Injection is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines. Vasopressin in Sodium Chloride Injection is indicated to increase blood pressure in adults with vasodilatory shock who remain hypotensive despite fluids and catecholamines. ( 1 )
Dosage & Administration
This product does not require further dilution prior to administration. ( 2.1 ) Post-cardiotomy shock: 0.03 units/minute to 0.1 units/minute by intravenous infusion ( 2.2 ) Septic shock: 0.01 units/minute to 0.07 units/minute by intravenous infusion ( 2.2 ) 2.1 Preparation of Solution Inspect parenteral drug products for particulate matter and discoloration prior to use, whenever solution and container permit. This product does not require further dilution prior to administration. 2.2 Administration In general, titrate to the lowest dose compatible with a clinically acceptable response. The recommended starting dose is: Post-cardiotomy shock: 0.03 units/minute by intravenous infusion Septic Shock: 0.01 units/minute by intravenous infusion Titrate up by 0.005 units/minute at 10- to 15-minute intervals until the target blood pressure is reached. There are limited data for doses above 0.1 units/minute for postcardiotomy shock and 0.07 units/minute for septic shock. Adverse reactions are expected to increase with higher doses. After target blood pressure has been maintained for 8 hours without the use of catecholamines, taper Vasopressin in Sodium Chloride Injection by 0.005 units/minute every hour as tolerated to maintain target blood pressure.
Warnings & Precautions
Can worsen cardiac function. ( 5.1 ) Reversible diabetes insipidus ( 5.2 ) 5.1 Worsening Cardiac Function A decrease in cardiac index may be observed with the use of vasopressin. 5.2 Reversible Diabetes Insipidus Patients may experience reversible diabetes insipidus, manifested by the development of polyuria, a dilute urine, and hypernatremia, after cessation of treatment with vasopressin. Monitor serum electrolytes, fluid status and urine output after vasopressin discontinuation. Some patients may require readministration of vasopressin or administration of desmopressin to correct fluid and electrolyte shifts.
Contraindications
Vasopressin in Sodium Chloride Injection is contraindicated in patients with known allergy or hypersensitivity to 8-L-arginine vasopressin or chlorobutanol. Vasopressin in Sodium Chloride Injection is contraindicated in patients with known allergy or hypersensitivity to 8-L-arginine vasopressin or chlorobutanol. ( 4 )
Adverse Reactions
The following adverse reactions associated with the use of vasopressin were identified in the literature. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to estimate their frequency reliably or to establish a causal relationship to drug exposure. Bleeding/lymphatic system disorders: Hemorrhagic shock, decreased platelets, intractable bleeding Cardiac disorders: Right heart failure, atrial fibrillation, bradycardia, myocardial ischemia Gastrointestinal disorders: Mesenteric ischemia Hepatobiliary: Increased bilirubin levels Renal/urinary disorders: Acute renal insufficiency Vascular disorders: Distal limb ischemia Metabolic: Hyponatremia Skin: Ischemic lesions The most common adverse reactions include decreased cardiac output, bradycardia, tachyarrhythmias, hyponatremia and ischemia (coronary, mesenteric, skin, digital). ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Long Grove Pharmaceuticals LLC at 1-855-642-2594 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Postmarketing Experience Reversible diabetes insipidus [see Warnings and Precautions ( 5.2 )]
Drug Interactions
Pressor effects of catecholamines and Vasopressin in Sodium Chloride Injection are expected to be additive. ( 7.1 ) Indomethacin may prolong effects of Vasopressin in Sodium Chloride Injection. ( 7.2 ) Co-administration of ganglionic blockers or drugs causing SIADH may increase the pressor response. ( 7.3 , 7.4 ) Co-administration of drugs causing diabetes insipidus may decrease the pressor response. ( 7.5 ) 7.1 Catecholamines Use with catecholamines is expected to result in an additive effect on mean arterial blood pressure and other hemodynamic parameters. Hemodynamic monitoring is recommended; adjust the dose of vasopressin as needed. 7.2 Indomethacin Use with indomethacin may prolong the effect of Vasopressin in Sodium Chloride Injection on cardiac index and systemic vascular resistance. Hemodynamic monitoring is recommended; adjust the dose of vasopressin as needed [ see Clinical Pharmacology ( 12.3 ) ]. 7.3 Ganglionic Blocking Agents Use with ganglionic blocking agents may increase the effect of Vasopressin in Sodium Chloride Injection on mean arterial blood pressure. Hemodynamic monitoring is recommended; adjust the dose of vasopressin as needed [ see Clinical Pharmacology ( 12.3 ) ]. 7.4 Drugs Suspected of Causing SIADH Use with drugs suspected of causing SIADH (e.g., SSRIs, tricyclic antidepressants, haloperidol, chlorpropamide, enalapril, methyldopa, pentamidine, vincristine, cyclophosphamide, ifosfamide, felbamate) may increase the pressor effect in addition to the antidiuretic effect of Vasopressin in Sodium Chloride Injection. Hemodynamic monitoring is recommended; adjust the dose of vasopressin as needed. 7.5 Drugs Suspected of Causing Diabetes Insipidus Use with drugs suspected of causing diabetes insipidus (e.g., demeclocycline, lithium, foscarnet, clozapine) may decrease the pressor effect in addition to the antidiuretic effect of Vasopressin in Sodium Chloride Injection. Hemodynamic monitoring is recommended; adjust the dose of vasopressin as needed.
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