Hydralazine Hydrochloride
- Product NDC
- 70518-1868
- 11-digit product format
- 705181868
- Labeler code
- 70518
- Product ID
- 70518-1868_81dd3355-f147-310c-e053-2991aa0a3366
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA088468
- Marketing category
- ANDA
- Marketing start
- 2019-02-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record