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AMLODIPINE AND VALSARTAN

NDC 43386-083 · Lupin Pharmaceuticals,Inc.

Generic nameAmlodipine and Valsartan
Dosage formTABLET
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, VALSARTAN
Strength5; 160 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Marketing categoryANDA

Packages

43386-083-03 — 30 TABLET in 1 BOTTLE (43386-083-03)

43386-083-09 — 90 TABLET in 1 BOTTLE (43386-083-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42806-055 — AMLODIPINE BESYLATE, 42806-056 — AMLODIPINE BESYLATE, 42806-057 — AMLODIPINE BESYLATE, 43063-041 — Amlodipine besylate, 43063-564 — Amlodipine besylate, 43063-764 — AMLODIPINE BESYLATE, 43353-989 — Amlodipine besylate, 43386-080 — amlodipine and valsartan, 43386-081 — amlodipine and valsartan, 43386-082 — amlodipine and valsartan, 43489-100 — Amlodipine Besylate, 43489-101 — Amlodipine Besylate, 43489-102 — Amlodipine Besylate, 43547-311 — valsartan and hydrochlorothiazide, 43547-312 — valsartan and hydrochlorothiazide, 43547-313 — valsartan and hydrochlorothiazide, 43547-314 — valsartan and hydrochlorothiazide, 43547-315 — valsartan and hydrochlorothiazide, 43547-367 — valsartan, 43547-368 — valsartan, +865 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