VASOPRESSIN
- Product NDC
- 42367-570
- 11-digit product format
- 423670570
- Labeler code
- 42367
- Product ID
- 42367-570_60d461a7-78b5-405d-b0c3-3c4fceadc566
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VASOPRESSIN
- Dosage form
- INJECTION
- Route
- PARENTERAL
- Labeler
- Eagle Pharmaceuticals, Inc.
- Application
- ANDA211538
- Marketing category
- ANDA
- Marketing start
- 2022-01-10
- Marketing end
- 0000-00-00
- Substance
- VASOPRESSIN
- Active strength
- 20 U/mL
- Pharmacologic classes
- Decreased Diuresis [PE], Vasoconstriction [PE], Vasopressins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42367-570-87 | 42367057087 | 25 VIAL, MULTI-DOSE in 1 CARTON (42367-570-87) > 1 mL in 1 VIAL, MULTI-DOSE (42367-570-22) | 2022-01-10 | 0000-00-00 | No | No | Current |