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Oxycodone and Acetaminophen

NDC 43386-492 · Lupin Pharmaceuticals,Inc.

Generic nameOxycodone and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength325; 7.5 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43386-356 — Hydrocodone Bitartrate and Acetaminophen, 43386-357 — Hydrocodone Bitartrate and Acetaminophen, 43386-358 — Hydrocodone Bitartrate and Acetaminophen, 43386-430 — Oxycodone Hydrochloride, 43386-431 — Oxycodone Hydrochloride, 43386-432 — Oxycodone Hydrochloride, 43386-433 — Oxycodone Hydrochloride, 43386-434 — Oxycodone Hydrochloride, 43386-490 — Oxycodone and Acetaminophen, 43386-491 — Oxycodone and Acetaminophen, 43386-493 — Oxycodone and Acetaminophen, 43386-920 — Oxycodone Hydrochloride, 43547-686 — butalbital, acetaminophen and caffeine, 43598-052 — Acetaminophen and Ibuprofen, 43602-190 — OXYCODONE HYDROCHLORIDE, 43602-198 — OXYCODONE HYDROCHLORIDE, 44567-340 — acetaminophen, 45802-201 — Acetaminophen, 45802-730 — Acetaminophen, 45802-732 — 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.