HYDRALAZINE HYDROCHLORIDE
- Product NDC
- 71335-0594
- 11-digit product format
- 713350594
- Labeler code
- 71335
- Product ID
- 71335-0594_29b07c22-e577-427c-bc6e-7a5d7e2c44ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydralazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA086242
- Marketing category
- ANDA
- Marketing start
- 2007-04-06
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 100 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0594-1 | 71335059401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0594-1) | 2017-11-21 | 0000-00-00 | No | No | Current |
| 71335-0594-2 | 71335059402 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0594-2) | 2017-11-21 | 0000-00-00 | No | No | Current |
| 71335-0594-3 | 71335059403 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0594-3) | 2017-11-21 | 0000-00-00 | No | No | Current |