Hydrocodone Bitartrate and Ibuprofen

NDC 13107-004 · Aurolife Pharma, LLC

Generic nameHydrocodone Bitartrate and Ibuprofen

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)HYDROCODONE BITARTRATE, IBUPROFEN

Strength7.5; 200 mg/1; mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA]

DEA scheduleCII

Marketing categoryANDA

Packages

13107-004-01 — 100 TABLET, FILM COATED in 1 BOTTLE (13107-004-01)

13107-004-05 — 500 TABLET, FILM COATED in 1 BOTTLE (13107-004-05)

13107-004-11 — 10 TABLET, FILM COATED in 1 BOTTLE (13107-004-11)

13107-004-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-3307 — Ibuprofen, 11822-4258 — Ibuprofen, 11822-4461 — Ibuprofen, 11822-5777 — Acetaminophen, Ibuprofen, 11822-6604 — Ibuprofen, 11822-7891 — IBUPROFEN, 11822-7892 — IBUPROFEN, 11822-7893 — IBUPROFEN, 11822-8925 — IBUPROFEN, 11822-9998 — Ibuprofen, 13107-019 — Hydrocodone Bitartrate and Acetaminophen, 13107-020 — Hydrocodone Bitartrate and Acetaminophen, 13107-021 — Hydrocodone Bitartrate and Acetaminophen, 13107-211 — Hydrocodone Bitartrate and Acetaminophen, 13107-212 — Hydrocodone Bitartrate and Acetaminophen, 13107-213 — Hydrocodone Bitartrate and Acetaminophen, 17856-5309 — Ibuprofen, 17856-5310 — Ibuprofen, 21130-006 — Ibuprofen, 21130-032 — Ibuprofen, +1553 more

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