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oxycodone and acetaminophen

NDC 72887-681 · FH2 Pharma LLC

Generic nameoxycodone and acetaminophen tablets
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength300; 5 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

72887-681-03 — 30 TABLET in 1 BOTTLE, PLASTIC (72887-681-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72865-115 — Oxycodone and Acetaminophen, 72865-116 — Oxycodone and Acetaminophen, 72865-128 — Oxycodone Hydrochloride, 72865-129 — Oxycodone Hydrochloride, 72865-201 — Hydrocodone Bitartrate and Acetaminophen, 72865-202 — Hydrocodone Bitartrate and Acetaminophen, 72865-203 — Hydrocodone Bitartrate and Acetaminophen, 72865-204 — Hydrocodone Bitartrate and Acetaminophen, 72887-193 — oxycodone and acetaminophen, 72887-648 — oxycodone hydrochloride and acetaminophen, 72887-682 — oxycodone and acetaminophen, 72887-683 — oxycodone and acetaminophen tablets, 72888-459 — Acetaminophen, 72988-0027 — ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, 72988-0032 — Acetaminophen, Caffeine Anhydrous,, 72988-0033 — Acetaminophen, CHLORPHENIRAMINE MALEATE, 72988-0036 — Acetaminophen, Isopropylantipyrine, 72988-0040 — Acetaminophen, Dried cinnamon Extract, 73057-350 — Acetaminophen 500mg, 73057-352 — Acetaminophen 500mg / Diphenhydramine HCl 25mg, +3633 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels