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Arthritis Pain Relief

NDC 68016-303 · CHAIN DRUG CONSORTIUM

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

Packages

68016-303-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68016-303-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67751-211 — Ibuprofen, Acetaminophen, 67751-215 — Acetaminophen, Aspirin, Caffeine, 67751-217 — chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, 67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 67751-241 — acetaminophen and diphenhydramine hydrochloride, 67751-243 — Acetaminophen, Aspirin, and Caffeine, 68001-495 — Acetaminophen, 68016-154 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 68016-198 — Acetaminophen, 68016-543 — Acetaminophen, 68016-654 — Acetaminophen Diphenhydramine HCl, 68016-734 — Acetaminophen, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68016-878 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 68047-721 — butalbital and acetaminophen, 68047-752 — butalbital and acetaminophen, 68047-753 — butalbital and acetaminophen, 68071-2494 — Hydrocodone Bitartrate and Acetaminophen, +3478 more