Hydralazine Hydrochloride
- Product NDC
- 50090-4641
- 11-digit product format
- 500904641
- Labeler code
- 50090
- Product ID
- 50090-4641_58cba237-99ae-414a-85ad-a1ae319bb0a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydralazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA086242
- Marketing category
- ANDA
- Marketing start
- 2007-04-06
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4641-0 | 50090464100 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-4641-0) | 2019-10-23 | 0000-00-00 | No | No | Current |
| 50090-4641-4 | 50090464104 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-4641-4) | 2019-10-23 | 0000-00-00 | No | No | Current |
| 50090-4641-5 | 50090464105 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4641-5) | 2019-10-23 | 0000-00-00 | No | No | Current |