Hydralazine Hydrochloride
- Product NDC
- 50090-6608
- 11-digit product format
- 500906608
- Labeler code
- 50090
- Product ID
- 50090-6608_29ea9739-73f0-4dc5-9392-8088957cb30c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA088468
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 50090-6608-0 | 50090660800 | 90 TABLET in 1 BOTTLE (50090-6608-0) | 90 tablet | 2023-08-22 | No | No | Historical |