Hydralazine Hydrochloride
- Product NDC
- 50090-2423
- 11-digit product format
- 500902423
- Labeler code
- 50090
- Product ID
- 50090-2423_7a751835-7a97-4b1f-a85d-336ca80372a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090527
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record