Hydralazine Hydrochloride
- Product NDC
- 71872-7268
- 11-digit product format
- 718727268
- Labeler code
- 71872
- Product ID
- 71872-7268_fab75f84-ce38-985f-e053-6294a90a6986
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDRALAZINE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA040388
- Marketing category
- ANDA
- Marketing start
- 2001-09-05
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FD171B778Y | HYDRALAZINE HYDROCHLORIDE | 304-20-1 | HYDRALAZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7268-1 | 71872726801 | 1 VIAL, SINGLE-USE in 1 BAG (71872-7268-1) / 1 mL in 1 VIAL, SINGLE-USE | 2001-10-11 | No | No | Historical |