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Valsartan

NDC 62332-045 · Alembic Pharmaceuticals Inc.

Generic nameValsartan
Dosage formTABLET
RouteORAL
Active ingredient(s)VALSARTAN
Strength80 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

62332-045-10 — 100 TABLET in 1 CARTON (62332-045-10)

62332-045-30 — 30 TABLET in 1 BOTTLE (62332-045-30)

62332-045-71 — 500 TABLET in 1 BOTTLE (62332-045-71)

62332-045-90 — 90 TABLET in 1 BOTTLE (62332-045-90)

62332-045-91 — 1000 TABLET in 1 BOTTLE (62332-045-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60290-085 — Sacubitril and Valsartan, 60290-086 — Sacubitril and Valsartan, 60290-087 — Sacubitril and Valsartan, 60687-612 — Valsartan, 60687-623 — Valsartan, 60687-634 — Valsartan, 60687-955 — Sacubitril and Valsartan, 60687-966 — Sacubitril and Valsartan, 60687-977 — Sacubitril and Valsartan, 62332-044 — Valsartan, 62332-046 — Valsartan, 62332-047 — Valsartan, 62332-079 — Valsartan and Hydrochlorothiazide, 62332-080 — Valsartan and Hydrochlorothiazide, 62332-081 — Valsartan and Hydrochlorothiazide, 62332-082 — Valsartan and Hydrochlorothiazide, 62332-083 — Valsartan and Hydrochlorothiazide, 62332-205 — Amlodipine and Valsartan, 62332-206 — Amlodipine and Valsartan, 62332-207 — Amlodipine and Valsartan, +387 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.