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basic care acid reducer

NDC 72288-329 · Amazon.com Services LLC

Generic namefamotidine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)FAMOTIDINE
Strength20 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

72288-329-78 — 1 BOTTLE in 1 CARTON (72288-329-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-543 — Famotidine, 72189-641 — Ibuprofen Famotidine, 72189-667 — Ibuprofen Famotidine, 72205-145 — Famotidine, 72205-146 — Famotidine, 72205-233 — FAMOTIDINE, 72288-141 — Famotidine, 72288-151 — famotidine, 72288-194 — Famotidine, 72288-321 — famotidine, calcium carbonate and magnesium hydroxide, 72288-363 — Famotidine, 72288-774 — famotidine, calcium carbonate and magnesium hydroxide, 72476-150 — famotidine, 72476-299 — famotidine, 72559-032 — Famotidine 20 mg, 72559-038 — Famotidine, 72578-214 — Ibuprofen and Famotidine, 72603-171 — Famotidine, 72657-112 — Famotidine, 72657-113 — Famotidine, +401 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