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Oxycodone and Acetaminophen

NDC 49999-852 · Quality Care products LLC

Generic nameOxycodone and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength325; 5 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

49999-852-14 — 14 TABLET in 1 BOTTLE, PLASTIC (49999-852-14)

49999-852-30 — 30 TABLET in 1 BOTTLE, PLASTIC (49999-852-30)

49999-852-60 — 60 TABLET in 1 BOTTLE, PLASTIC (49999-852-60)

49999-852-90 — 90 TABLET in 1 BOTTLE, PLASTIC (49999-852-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49580-0685 — Acetaminophen, 49580-0821 — Acetaminophen, 49580-2880 — Acetaminophen, 49580-3278 — Acetaminophen, 49580-4160 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine HCI, 49873-082 — acetaminophen, 49873-108 — acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, 49873-113 — acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride, 49873-114 — acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride, 49999-060 — ACETAMINOPHEN AND CODEINE PHOSPHATE, 49999-899 — Oxycodone Hydchloride, 50066-302 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 50066-303 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and DOXYLAMINE SUCCINATE, 50066-313 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 50066-516 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 50066-519 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 50066-520 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 50066-525 — ACETAMINOPHEN, 50066-630 — acetaminophen, aspirin, and caffeine, 50090-0001 — 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.