Acetaminophen

NDC 0121-1314 · PAI Holdings, LLC dba PAI Pharma

Generic nameAcetaminophen

Dosage formSOLUTION

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength325 mg/10.15mL

Marketing categoryOTC MONOGRAPH DRUG

Packages

0121-1314-00 — 10 TRAY in 1 CASE (0121-1314-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10.15 mL in 1 CUP, UNIT-DOSE (0121-1314-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-6012 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 0113-7019 — acetaminophen, dextromethorphan hydrobromide, 0113-8959 — Acetaminophen, 0113-9523 — Acetaminophen, 0121-0504 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-0657 — Acetaminophen, 0121-0941 — Acetaminophen, 0121-0966 — Acetaminophen, 0121-1008 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-1047 — Acetaminophen, 0121-1544 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0121-1781 — Acetaminophen, 0121-1882 — Acetaminophen, 0121-1971 — Acetaminophen, 0121-2094 — Acetaminophen, 0121-2316 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0121-2823 — Acetaminophen, 0121-3141 — Acetaminophen, 0121-4772 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0135-0537 — acetaminophen, +3478 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.