Hydralazine Hydrochloride
- Product NDC
- 70518-4007
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040858
- Marketing category
- ANDA
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70518-4007-0 | 30 TABLET in 1 BLISTER PACK (70518-4007-0) | 2024-02-01 | No | Historical | |
| 70518-4007-1 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4007-1) | 2025-05-29 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| ​HYDRALAZINE HYDROCHLORIDE TABLETS, USP ​ | REMEDYREPACK INC. | 2025-05-29 | HUMAN PRESCRIPTION DRUG LABEL | 3 |