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Ibuprofen

NDC 62207-356 · Granules India Limited

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

62207-356-42 — 50 TABLET, FILM COATED in 1 BOTTLE (62207-356-42)

62207-356-43 — 100 TABLET, FILM COATED in 1 BOTTLE (62207-356-43)

62207-356-47 — 500 TABLET, FILM COATED in 1 BOTTLE (62207-356-47)

62207-356-49 — 1000 TABLET, FILM COATED in 1 BOTTLE (62207-356-49)

62207-356-54 — 30 TABLET, FILM COATED in 1 BOTTLE (62207-356-54)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62011-0070 — Ibuprofen and Pseudoephedrine Hydrochloride, 62011-0368 — Ibuprofen, 62011-0399 — Ibuprofen, 62135-400 — Ibuprofen, 62135-401 — Ibuprofen, 62135-402 — Ibuprofen, 62207-320 — IBUPROFEN, 62207-321 — IBUPROFEN, 62207-354 — Ibuprofen, 62207-355 — Ibuprofen, 62207-365 — Ibuprofen, 62207-366 — Ibuprofen, 62207-395 — Ibuprofen, 62207-396 — Ibuprofen, 62936-0941 — ibuprofen, 63187-022 — Ibuprofen, 63187-451 — ibuprofen, 63187-489 — Ibuprofen, 63187-527 — Ibuprofen, 63187-614 — Ibuprofen, +1311 more

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