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Hydrocodone Bitartrate and Acetaminophen

NDC 87063-049 · Asclemed USA, Inc.

Generic nameHydrocodone Bitartrate and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCODONE BITARTRATE, ACETAMINOPHEN
Strength325; 5 mg/1; mg/1
Pharmacologic classOpioid Agonist [EPC], Opioid Agonists [MoA]
DEA scheduleCII
Marketing categoryANDA

Packages

87063-049-01 100 TABLET in 1 BOTTLE (87063-049-01)

87063-049-05 5 TABLET in 1 BOTTLE (87063-049-05)

87063-049-07 7 TABLET in 1 BOTTLE (87063-049-07)

87063-049-10 10 TABLET in 1 BOTTLE (87063-049-10)

87063-049-14 14 TABLET in 1 BOTTLE (87063-049-14)

87063-049-20 20 TABLET in 1 BOTTLE (87063-049-20)

87063-049-30 30 TABLET in 1 BOTTLE (87063-049-30)

87063-049-60 60 TABLET in 1 BOTTLE (87063-049-60)

87063-049-90 90 TABLET in 1 BOTTLE (87063-049-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

85828-417 — Acetaminophen 325mg/ Dextromethorphan HBr 10mg/ Phenylephrine HCl 5mg, 85828-418 — Nighttime Cold and Flu Relief, 85828-750 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 85828-772 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine HCl, 85828-774 — Acetaminophen,Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 85828-775 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 85828-922 — Acetaminophen, 87063-032 — oxycodone and acetaminophen, 87063-033 — oxycodone and acetaminophen, 87063-034 — oxycodone and acetaminophen, 87063-050 — Hydrocodone Bitartrate and Acetaminophen, 87063-051 — Hydrocodone Bitartrate and Acetaminophen, 87063-222 — Acetaminophen, 87078-121 — Acetaminophen 160 mg / 5 mL, 87078-131 — Acetaminophen, 87078-331 — Acetaminophen 325 mg and Dextromethorphan HBr 10 mg Oral Liquid Day Time Kids, 87078-872 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCI, 87078-972 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 87339-001 — ACETAMINOPHEN, 87438-0001 — Acetaminophen, +3514 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