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Valsartan

NDC 51655-834 · Northwind Health Company, LLC

Generic nameValsartan
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VALSARTAN
Strength160 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

51655-834-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-834-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-936 — sacubitril and valsartan, 51407-937 — sacubitril and valsartan, 51655-243 — valsartan and hydrochlorothiazide, 51655-244 — valsartan, 51655-389 — valsartan and hydrochlorothiazide, 51655-456 — Valsartan, 51655-653 — valsartan, 51655-655 — Valsartan and Hydrochlorothiazide, 51655-695 — valsartan, 51655-698 — Valsartan and Hydrochlorothiazide, 51660-140 — VALSARTAN, 51660-141 — VALSARTAN, 51660-142 — VALSARTAN, 51660-143 — VALSARTAN, 53746-837 — Valsartan, 53746-838 — Valsartan, 53746-839 — Valsartan, 53746-840 — Valsartan, 53746-845 — Valsartan and Hydrochlorothiazide, 53746-846 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels