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Oxycodone Hydrochloride and Acetaminophen

NDC 64850-622 · Elite Laboratories, Inc.

Generic nameOxycodone Hydrochloride 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

64850-622-01 — 100 TABLET in 1 BOTTLE (64850-622-01)

64850-622-05 — 500 TABLET in 1 BOTTLE (64850-622-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64380-261 — Oxycodone Hydrochloride, 64380-262 — Oxycodone Hydrochloride, 64380-263 — Oxycodone Hydrochloride, 64380-440 — hydrocodone bitartrate and acetaminophen, 64380-441 — hydrocodone bitartrate and acetaminophen, 64380-442 — hydrocodone bitartrate and acetaminophen, 64380-446 — Acetaminophen and Codeine Phosphate, 64380-447 — Acetaminophen and Codeine Phosphate, 64380-448 — Acetaminophen and Codeine Phosphate, 64850-621 — Oxycodone Hydrochloride and Acetaminophen, 64850-623 — Oxycodone Hydrochloride and Acetaminophen, 64850-630 — Hydrocodone Bitartrate and Acetaminophen, 64850-631 — Hydrocodone Bitartrate and Acetaminophen, 64850-632 — Hydrocodone Bitartrate and Acetaminophen, 64850-633 — Hydrocodone Bitartrate and Acetaminophen, 64850-641 — Acetaminophen and Codeine Phosphate, 64850-642 — Acetaminophen and Codeine Phosphate, 64850-643 — Acetaminophen and Codeine Phosphate, 64950-290 — Butalbital, Acetaminophen, and Caffeine, 64950-343 — hydrocodone bitartrate 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.