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Hydrocodone Bitartrate and Acetaminophen

NDC 0121-2316 · PAI Holdings, LLC dba PAI Pharma

Generic nameHYDROCODONE BITARTRATE and ACETAMINOPHEN

Dosage formSOLUTION

RouteORAL

Active ingredient(s)HYDROCODONE BITARTRATE, ACETAMINOPHEN

Strength325; 7.5 mg/15mL; mg/15mL

Pharmacologic classOpioid Agonist [EPC], Opioid Agonists [MoA]

DEA scheduleCII

Marketing categoryANDA

Packages

0121-2316-50 — 5 TRAY in 1 CASE (0121-2316-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-0966 — Acetaminophen, 0121-1008 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-1036 — Hydrocodone Bitartrate and Homatropine Methylbromide, 0121-1047 — Acetaminophen, 0121-1314 — Acetaminophen, 0121-1544 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0121-1781 — Acetaminophen, 0121-1882 — Acetaminophen, 0121-1971 — Acetaminophen, 0121-2094 — Acetaminophen, 0121-2823 — Acetaminophen, 0121-3141 — Acetaminophen, 0121-4772 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0135-0537 — acetaminophen, 0135-0539 — acetaminophen, 0135-0578 — acetaminophen, chlorpheniramine maleate, phenylephrine hcl, 0135-0607 — acetaminophen and phenyleprine HCl, 0135-0608 — acetaminophen and diphenhydramine HCl, 0135-0609 — acetaminophen, 0135-0620 — acetaminophen and caffeine, +3514 more

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