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Ibuprofen PM

NDC 21130-056 · Safeway, Inc.

Generic nameDiphenhydramine Citrate, Ibuprofen
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)IBUPROFEN, DIPHENHYDRAMINE CITRATE
Strength38; 200 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

21130-056-40 — 1 BOTTLE, PLASTIC in 1 BOX (21130-056-40) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC

21130-056-80 — 1 BOTTLE, PLASTIC in 1 BOX (21130-056-80) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-7891 — IBUPROFEN, 11822-7892 — IBUPROFEN, 11822-7893 — IBUPROFEN, 11822-8925 — IBUPROFEN, 11822-9998 — Ibuprofen, 13107-004 — Hydrocodone Bitartrate and Ibuprofen, 17856-5309 — Ibuprofen, 17856-5310 — Ibuprofen, 21130-006 — Ibuprofen, 21130-032 — Ibuprofen, 21130-070 — Ibuprofen, 21130-216 — IBUPROFEN, 21130-220 — Ibuprofen, 21130-228 — Ibuprofen and Diphenhydramine Citrate, 21130-261 — Ibuprofen, 21130-358 — Ibuprofen, 21130-359 — Ibuprofen, 21130-361 — Ibuprofen, 21130-393 — Ibuprofen, 21130-396 — Ibuprofen, +1316 more

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