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ACETAMINOPHEN

NDC 37835-512 · Bi-Mart

Generic nameACETAMINOPHEN
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength650 mg/1
Marketing categoryANDA

Packages

37835-512-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-512-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-775 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-792 — Acetaminophen, 37808-795 — Acetaminophen and Diphenhydramine Hydrochloride, 37808-811 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 37808-848 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37808-864 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37808-945 — Acetaminophen, 37808-980 — Acetaminophen, 37808-994 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37835-507 — Acetaminophen, 37835-520 — acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 37835-522 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 37835-524 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 37835-525 — Acetaminophen, Doxylamine succinate and Dextromethorphan HBr, 37835-526 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 37835-527 — acetaminophen, dextromethorphan HBr, Phenylephrine HCl, 37835-531 — Acetaminophen, Aspirin, and Caffeine, 37835-537 — Acetaminophen and Diphenhydramine Hydrochloride, 39328-031 — Acetaminophen, 39328-032 — Acetaminophen, +3476 more

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