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Valsartan

NDC 65162-840 · Amneal Pharmaceuticals LLC

Generic nameValsartan
Dosage formTABLET
RouteORAL
Active ingredient(s)VALSARTAN
Strength320 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

65162-840-09 — 90 TABLET in 1 BOTTLE (65162-840-09)

65162-840-11 — 1000 TABLET in 1 BOTTLE (65162-840-11)

65162-840-50 — 500 TABLET in 1 BOTTLE (65162-840-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64380-199 — amlodipine besylate valsartan hydrochlorothiazide, 64380-200 — amlodipine besylate valsartan hydrochlorothiazide, 64380-201 — amlodipine besylate valsartan hydrochlorothiazide, 64380-214 — amlodipine and valsartan, 64380-215 — amlodipine and valsartan, 64380-216 — amlodipine and valsartan, 64380-217 — amlodipine and valsartan, 65162-837 — Valsartan, 65162-838 — Valsartan, 65162-839 — Valsartan, 65162-845 — Valsartan and Hydrochlorothiazide, 65162-846 — Valsartan and Hydrochlorothiazide, 65162-847 — Valsartan and Hydrochlorothiazide, 65162-848 — Valsartan and Hydrochlorothiazide, 65162-849 — Valsartan and Hydrochlorothiazide, 65862-547 — Valsartan and Hydrochlorothiazide, 65862-548 — Valsartan and Hydrochlorothiazide, 65862-549 — Valsartan and Hydrochlorothiazide, 65862-550 — Valsartan and Hydrochlorothiazide, 65862-551 — Valsartan and Hydrochlorothiazide, +387 more

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