Hydralazine Hydrochloride
- Product NDC
- 0615-0516
- 11-digit product format
- 006150516
- Labeler code
- 0615
- Product ID
- 0615-0516_1cce9fcb-74f7-4f96-a546-5572b96d4d7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA087836
- Marketing category
- ANDA
- Marketing start
- 1982-10-05
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#