Details for New Drug Application (NDA): 217766
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The generic ingredient in VASOPRESSIN IN SODIUM CHLORIDE 0.9% is vasopressin. There are nine drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the vasopressin profile page.
Summary for 217766
| Tradename: | VASOPRESSIN IN SODIUM CHLORIDE 0.9% |
| Applicant: | Long Grove Pharms |
| Ingredient: | vasopressin |
| Patents: | 0 |
Pharmacology for NDA: 217766
| Physiological Effect | Decreased Diuresis Vasoconstriction |
Suppliers and Packaging for NDA: 217766
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| VASOPRESSIN IN SODIUM CHLORIDE 0.9% | vasopressin | SOLUTION;INTRAVENOUS | 217766 | NDA | Long Grove Pharmaceuticals, LLC | 81298-8552 | 81298-8552-3 | 10 VIAL, SINGLE-DOSE in 1 CARTON (81298-8552-3) / 100 mL in 1 VIAL, SINGLE-DOSE (81298-8552-1) |
| VASOPRESSIN IN SODIUM CHLORIDE 0.9% | vasopressin | SOLUTION;INTRAVENOUS | 217766 | NDA | Long Grove Pharmaceuticals, LLC | 81298-8554 | 81298-8554-3 | 10 VIAL, SINGLE-DOSE in 1 CARTON (81298-8554-3) / 100 mL in 1 VIAL, SINGLE-DOSE (81298-8554-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 20UNITS/100ML (0.2UNITS/ML) | ||||
| Approval Date: | Jul 11, 2024 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;INTRAVENOUS | Strength | 40UNITS/100ML (0.4UNITS/ML) | ||||
| Approval Date: | Jul 11, 2024 | TE: | RLD: | Yes | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION;INTRAVENOUS | Strength | 50UNITS/50ML (1UNIT/ML) | ||||
| Approval Date: | Jul 11, 2024 | TE: | RLD: | Yes | |||||
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