NDC 71335-9756 – Hydralazine Hydrochloride
Hydralazine Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC71335-9756
Product details
- Brand name
- Hydralazine Hydrochloride
- Generic name
- Hydralazine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205236
- Marketed since
- May 26, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Arteriolar Vasodilator
Active ingredients
- Hydralazine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Hydralazine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9756-1 | 30 TABLET in 1 BOTTLE (71335-9756-1) | Jul 25, 2023 |
| 71335-9756-2 | 60 TABLET in 1 BOTTLE (71335-9756-2) | Jul 25, 2023 |
| 71335-9756-3 | 120 TABLET in 1 BOTTLE (71335-9756-3) | Jul 25, 2023 |
| 71335-9756-4 | 90 TABLET in 1 BOTTLE (71335-9756-4) | Jul 25, 2023 |
| 71335-9756-5 | 10 TABLET in 1 BOTTLE (71335-9756-5) | Jul 25, 2023 |
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