NDC 70771-1488-0
valsartan and hydrochlorothiazide 12.5 mg/1
valsartan and hydrochlorothiazide · TABLET, FILM COATED
valsartan and hydrochlorothiazide is a tablet, film coated containing valsartan and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Zydus Lifesciences Limited.
Key Facts
- Brand Name
- valsartan and hydrochlorothiazide
- Generic Name
- valsartan and hydrochlorothiazide
- NDC Code (Package)
70771-1488-0- NDC Code (Product)
70771-1488- Manufacturer
- Zydus Lifesciences Limited
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA203000
- Drug Class
- Thiazide Diuretic [EPC]; Angiotensin 2 Receptor Blocker [EPC]
- Marketing Start
- 02/12/2020
Recall History
No Recall HistoryView Full Drug Page
valsartan and hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.