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Pain Relief

NDC 55910-812 · DOLGENCORP, LLC

Generic nameAcetaminophen

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength500 mg/1

Marketing categoryOTC MONOGRAPH DRUG

Packages

55910-812-32 — 120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-686 — Acetaminophen, Aspirin, Caffeine, 55910-697 — Acetaminophen, 55910-701 — Acetaminophen, 55910-716 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine HCI, 55910-737 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 55910-738 — Acetaminophen, 55910-749 — Acetaminophen, 55910-753 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 55910-757 — Acetaminophen, Guaifenesin, Phenylephrine HCL, 55910-801 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL, 55910-828 — Acetaminophen, 55910-834 — Acetaminophen, Diphenhydramine HCl, 55910-886 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-892 — Acetaminophen, 55910-895 — Acetaminophen, 55910-900 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 55910-910 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 55910-925 — Acetaminophen, Phenylephrine HCl, 55910-927 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 55910-928 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, +3476 more

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