Ibuprofen and Famotidine

NDC 72578-214 · Viona Pharmaceuticals Inc

Generic nameIbuprofen and Famotidine

Dosage formTABLET

RouteORAL

Active ingredient(s)IBUPROFEN, FAMOTIDINE

Strength26.6; 800 mg/1; mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

Marketing categoryANDA

Packages

72578-214-16 — 90 TABLET in 1 BOTTLE (72578-214-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72476-150 — famotidine, 72476-231 — Acetaminophen, Ibuprofen, 72476-299 — famotidine, 72476-358 — Ibuprofen, 72476-365 — Ibuprofen, 72476-366 — Ibuprofen, 72476-745 — Ibuprofen, 72476-843 — Ibuprofen, 72559-032 — Famotidine 20 mg, 72559-038 — Famotidine, 72603-171 — Famotidine, 72603-909 — Ibuprofen, 72603-910 — Ibuprofen, 72657-112 — Famotidine, 72657-113 — Famotidine, 72657-132 — Famotidine, 72657-157 — Acetaminophen, Ibuprofen, 72789-185 — Ibuprofen, 72789-186 — Ibuprofen, 72789-187 — Ibuprofen, +1712 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