Hydralazine Hydrochloride
- Product NDC
- 72162-1521
- 11-digit product format
- 721621521
- Labeler code
- 72162
- Product ID
- 72162-1521_2b4aae2f-2c3f-4ff8-9a1d-4c51c9b7f19d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA088467
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1521-0 | 72162152100 | 1000 TABLET in 1 BOTTLE (72162-1521-0) | 1000 tablet | 2024-12-24 | No | No | Historical |