Hydralazine Hydrochloride
- Product NDC
- 55154-2083
- 11-digit product format
- 551542083
- Labeler code
- 55154
- Product ID
- 55154-2083_76c05e84-b54b-4a61-8f62-fe944599c17f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA086242
- Marketing category
- ANDA
- Marketing start
- 2008-03-18
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-2083-0 | 55154208300 | 10 BLISTER PACK in 1 BAG (55154-2083-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2008-03-18 | 0000-00-00 | No | No | Current |