Vasopressin
- Product NDC
- 63323-302
- 11-digit product format
- 633230302
- Labeler code
- 63323
- Product ID
- 63323-302_9af1ae6c-e1ef-28ff-e053-2a95a90ac717
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VASOPRESSIN
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; SUBCUTANEOUS
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2001-07-17
- Marketing end
- 0000-00-00
- Substance
- VASOPRESSIN
- Active strength
- 20 [USP'U]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| VASOPRESSIN | ACTIVE INGREDIENT | Y87Y826H08 | VASOPRESSIN INJECTION, SOLUTION [FENERAL INJECTABLES & VACCINES, INC] | 1 | |
| VASOPRESSIN | ACTIVE MOIETY | Y87Y826H08 | VASOPRESSIN INJECTION, SOLUTION [FENERAL INJECTABLES & VACCINES, INC] | 1 | |
| ACETIC ACID | INACTIVE INGREDIENT | Q40Q9N063P | VASOPRESSIN INJECTION, SOLUTION [FENERAL INJECTABLES & VACCINES, INC] | 1 | |
| CHLOROBUTANOL | INACTIVE INGREDIENT | HM4YQM8WRC | VASOPRESSIN INJECTION, SOLUTION [FENERAL INJECTABLES & VACCINES, INC] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | VASOPRESSIN INJECTION, SOLUTION [FENERAL INJECTABLES & VACCINES, INC] | 1 | |
DailyMed RxNorm Mappings#