United States · FDA National Drug Code directory
valsartan and hydrochlorothiazide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70771-1485_be4934db-c496-4b06-84c6-587cb656d5fc
- Product NDC
- 70771-1485
- Form
- TABLET, FILM COATED
- Composition / generic term
- valsartan and hydrochlorothiazide
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200212
- Source listing expiry
- 20261231
Source-listed ingredients
- VALSARTAN — 80 mg/1
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1485-0) · 70771-1485-0
- 10 BLISTER PACK in 1 CARTON (70771-1485-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 70771-1485-4
- 90 TABLET, FILM COATED in 1 BOTTLE (70771-1485-9) · 70771-1485-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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