NDC 62332-079 – Valsartan and Hydrochlorothiazide
Valsartan 80 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC62332-079
Product details
- Brand name
- Valsartan and Hydrochlorothiazide
- Generic name
- Valsartan and Hydrochlorothiazide
- Labeler
- Alembic Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA201662
- Marketed since
- May 20, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Valsartan 80 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Valsartan and Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 62332-079-10 | 100 TABLET, FILM COATED in 1 CARTON (62332-079-10) | May 20, 2016 |
| 62332-079-30 | 30 TABLET, FILM COATED in 1 BOTTLE (62332-079-30) | May 20, 2016 |
| 62332-079-71 | 500 TABLET, FILM COATED in 1 BOTTLE (62332-079-71) | May 20, 2016 |
| 62332-079-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62332-079-90) | May 20, 2016 |
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