NDC 23155-834 – Hydralazine Hydrochloride
Hydralazine Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC23155-834
Product details
- Brand name
- Hydralazine Hydrochloride
- Generic name
- Hydralazine Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040858
- Marketed since
- August 2, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Arteriolar Vasodilator
Active ingredients
- Hydralazine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Hydralazine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 23155-834-01 | 100 TABLET in 1 BOTTLE (23155-834-01) | Aug 2, 2023 |
| 23155-834-10 | 1000 TABLET in 1 BOTTLE (23155-834-10) | Aug 2, 2023 |
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