Skip to main content

Oxycodone and Acetaminophen

NDC 31722-194 · Camber Pharmaceuticals, Inc.

Generic nameOxycodone and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength325; 10 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

31722-194-01 — 100 TABLET in 1 BOTTLE (31722-194-01)

31722-194-05 — 500 TABLET in 1 BOTTLE (31722-194-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 30142-766 — Acetaminophen, 30142-818 — Acetaminophen, 30142-828 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 30142-865 — Acetaminophen, Aspirin, Caffeine, 30142-896 — acetaminophen, aspirin, caffeine, 30142-988 — Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr, Phenylephrine HCl, 31722-191 — Oxycodone and Acetaminophen, 31722-192 — Oxycodone and Acetaminophen, 31722-193 — Oxycodone and Acetaminophen, 31722-205 — Acetaminophen, 31722-484 — Oxycodone Hydrochloride, 31722-485 — Oxycodone Hydrochloride, 31722-486 — Oxycodone Hydrochloride, 31722-917 — Oxycodone Hydrochloride, 31722-918 — Oxycodone Hydrochloride, 31722-940 — Hydrocodone Bitartrate and Acetaminophen, 31722-942 — Hydrocodone Bitartrate and Acetaminophen, 31722-948 — Oxycodone and Acetaminophen, 31722-949 — Oxycodone and Acetaminophen, +3633 more

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