Valsartan and Hydrochlorothiazide
- Product NDC
- 65162-846
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valsartan and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA204382
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE; VALSARTAN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 65162-846-03 | 30 TABLET, FILM COATED in 1 BOTTLE (65162-846-03) | 2023-08-14 | | No | Historical |
| 65162-846-09 | 90 TABLET, FILM COATED in 1 BOTTLE (65162-846-09) | 2023-08-14 | | No | Historical |
| 65162-846-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (65162-846-11) | 2023-08-14 | | No | Historical |
| 65162-846-50 | 500 TABLET, FILM COATED in 1 BOTTLE (65162-846-50) | 2023-08-14 | | No | Historical |