NDC 71335-0202 – Hydralazine Hydrochloride
Hydralazine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC71335-0202
Product details
- Brand name
- Hydralazine Hydrochloride
- Generic name
- Hydralazine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040901
- Marketed since
- January 1, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Arteriolar Vasodilator
Active ingredients
- Hydralazine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Hydralazine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0202-1 | 30 TABLET in 1 BOTTLE (71335-0202-1) | Jun 30, 2017 |
| 71335-0202-2 | 60 TABLET in 1 BOTTLE (71335-0202-2) | Jun 30, 2017 |
| 71335-0202-3 | 90 TABLET in 1 BOTTLE (71335-0202-3) | Jun 30, 2017 |
| 71335-0202-4 | 10 TABLET in 1 BOTTLE (71335-0202-4) | Jun 30, 2017 |
| 71335-0202-5 | 100 TABLET in 1 BOTTLE (71335-0202-5) | Jun 30, 2017 |
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