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Members Mark Arthritis Pain

NDC 68196-611 · Sam's West Inc

Generic nameacetaminophen

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength650 mg/1

Marketing categoryANDA

Packages

68196-611-82 — 200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68196-611-82)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68163-547 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 68163-695 — Acetaminophen, 68163-698 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 68163-737 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 68163-749 — Acetaminophen, Dextromethorphan HBr, 68196-031 — Acetaminophen, 68196-034 — Acetaminophen, 68196-177 — Acetaminophen, 68196-556 — acetaminophen, diphenhydramine HCl, 68196-606 — Acetaminophen, 68196-919 — acetaminophen, 68196-935 — Acetaminophen, 68210-4210 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 68210-5053 — Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68391-004 — Acetaminophen, 68391-288 — Acetaminophen, 68391-411 — Acetaminophen, 68391-430 — Acetaminophen, Diphenhydramine, 68391-659 — Acetaminophen, 68391-863 — Acetaminophen, Diphenhydramine HCL, +3476 more

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