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Combogesic

NDC 71335-3161 · Bryant Ranch Prepack

Generic nameACETAMINOPHEN and IBUPROFEN
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, IBUPROFEN
Strength325; 97.5 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryNDA

Packages

71335-3161-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-3161-1)

71335-3161-2 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-3161-2)

71335-3161-3 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-3161-3)

71335-3161-4 — 120 TABLET, FILM COATED in 1 BOTTLE (71335-3161-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2722 — Acetaminophen, 71335-2740 — Hydrocodone Bitartrate and Acetaminophen, 71335-2747 — Acetaminophen, 71335-2755 — Acetaminophen, 71335-2818 — Acetaminophen and Codeine Phosphate, 71335-2916 — Acetaminophen and Codeine Phosphate, 71335-2969 — Hydrocodone Bitartrate and Acetaminophen, 71335-3108 — Ibuprofen, 71335-3121 — Ibuprofen, 71335-3130 — ACETAMINOPHEN, 71335-9602 — Hydrocodone Bitartrate and Acetaminophen, 71335-9603 — Butalbital, Acetaminophen and Caffeine, 71335-9674 — oxycodone and acetaminophen, 71335-9675 — oxycodone and acetaminophen, 71335-9734 — Hydrocodone Bitartrate and Acetaminophen, 71335-9735 — Hydrocodone Bitartrate and Acetaminophen, 71335-9736 — Hydrocodone Bitartrate and Acetaminophen, 71335-9737 — Hydrocodone Bitartrate and Acetaminophen, 71335-9746 — Acetaminophen tablet extended release, 71399-0020 — Childrens Acetaminophen, +4731 more

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