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8 Hour Arthritis Pain

NDC 68998-401 · MARC GLASSMAN, INC.

Generic nameAcetaminophen

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength650 mg/1

Marketing categoryANDA

Packages

68998-401-03 — 1 BOTTLE, PLASTIC in 1 CARTON (68998-401-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68998-198 — Acetaminophen, 68998-219 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 68998-220 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 68998-228 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 68998-238 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 68998-263 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 68998-275 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 68998-301 — Acetaminophen, 68998-323 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 68998-392 — Acetaminophen, 68998-525 — ACETAMINOPHEN, 69168-001 — Tension Headache Relief, 69168-003 — Pain Relief PM, 69168-004 — Cold Medicine, 69168-005 — Pain Relief, 69168-010 — Acetaminophen 325mg, 69168-011 — Acetaminophen 500mg, 69168-029 — Tension Headache Relief, 69168-270 — Acetaminophen and Phenylephrine HCl, 69168-285 — Acetaminophen, Aspirin and Caffeine, +3476 more

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