VASOPRESSIN
- Product NDC
- 51662-1682
- 11-digit product format
- 516621682
- Labeler code
- 51662
- Product ID
- 51662-1682_5232a8bc-d7af-48a5-e063-6294a90a76ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VASOPRESSIN
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA212593
- Marketing category
- NDA
- Marketing start
- 2023-06-21
- Substance
- VASOPRESSIN
- Active strength
- 20 [USP'U]/mL
- Pharmacologic classes
- Decreased Diuresis [PE], Vasoconstriction [PE], Vasopressins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VASOPRESSIN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VASOPRESSIN | 20 [USP'U]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Y4907O6MFD |
| Rxcui | 313578 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1682-1 | VASOPRESSIN | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1682-1 | 51662168201 | 10 mL in 1 VIAL (51662-1682-1) | 10 ml | 2023-06-21 | No | No | Historical |