NDC 23155-003 – Hydralazine Hydrochloride
Hydralazine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC23155-003
Product details
- Brand name
- Hydralazine Hydrochloride
- Generic name
- Hydralazine hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA086242
- Marketed since
- April 6, 2007
- Marketing end
- September 30, 2026
- 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 |
|---|---|---|
| 23155-003-01 | 100 TABLET, FILM COATED in 1 BOTTLE (23155-003-01) | Apr 6, 2007 |
| 23155-003-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (23155-003-10) | Apr 6, 2007 |
Recalls mentioning this NDC
- D-0184-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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