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Ibuprofen PM

NDC 59640-020 · HEB

Generic nameIBUPROFEN, DIPHENHYDRAMINE HCL
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)IBUPROFEN, DIPHENHYDRAMINE HYDROCHLORIDE
Strength25; 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

59640-020-15 — 1 BOTTLE, PLASTIC in 1 CARTON (59640-020-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59450-174 — Acetaminophen, Diphenhydramine hydrochloride, 59450-295 — Diphenhydramine HCl, Zinc acetate, 59450-601 — Diphenhydramine hydrochloride, 59555-002 — DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate, 59556-764 — IBUPROFEN, 59556-855 — Ibuprofen, 59556-856 — Ibuprofen, 59556-857 — IBUPROFEN, 59556-858 — IBUPROFEN, 59556-895 — IBUPROFEN, 59640-090 — DIPHENHYDRAMINE HYDROCHLORIDE, 59651-032 — Ibuprofen Oral, 59651-360 — Ibuprofen, 59651-361 — Ibuprofen, 59651-362 — Ibuprofen, 59651-908 — Ibuprofen and famotidine, 59726-003 — Ibuprofen, 59726-046 — Ibuprofen, 59726-123 — Ibuprofen, 59726-139 — Ibuprofen, +2338 more

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