Acetaminophen

NDC 0121-0941 · PAI Holdings, LLC dba PAI Pharma

Generic nameAcetaminophen

Dosage formSUSPENSION

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength160 mg/5mL

Marketing categoryOTC MONOGRAPH DRUG

Packages

0121-0941-00 — 10 TRAY in 1 CASE (0121-0941-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0941-05)

0121-0941-94 — 3 TRAY in 1 CASE (0121-0941-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-0941-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0113-4500 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0113-5299 — acetaminophen, ibuprofen, 0113-5300 — Acetaminophen, Ibuprofen, 0113-5305 — acetaminophen, dextromethorphan hydrobromide, 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, 0121-0966 — Acetaminophen, 0121-1008 — ACETAMINOPHEN and CODEINE PHOSPHATE, 0121-1047 — Acetaminophen, 0121-1314 — Acetaminophen, 0121-1544 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, 0121-1781 — Acetaminophen, 0121-1882 — Acetaminophen, 0121-1971 — Acetaminophen, 0121-2094 — Acetaminophen, 0121-2316 — HYDROCODONE BITARTRATE and ACETAMINOPHEN, +3478 more

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