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Pain Reliever

NDC 71679-304 · Health Pharma USA LLC

Generic nameAcetaminophen

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength500 mg/1

Marketing categoryOTC MONOGRAPH DRUG

Packages

71679-304-00 — 31000 TABLET, FILM COATED in 1 DRUM (71679-304-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71399-0038 — Children Acetaminophen, 71399-0048 — Children Acetaminophen, 71399-1025 — Acetaminophen, 71399-1026 — Acetaminophen, 71444-793 — Acetaminophen, 71444-893 — Acetaminophen, 71594-702 — Acetaminophen 80 mg, 71610-238 — Acetaminophen, 71679-101 — acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 71679-102 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 71679-305 — Acetaminophen, 71687-3003 — Acetaminophen, Pamabrom, Pyrilamine maleate, 71687-3006 — Acetaminophen and Aspirin and Caffeine, 71687-3102 — Acetaminophen and Pamabrom and Pyrilamine maleate, 71930-019 — Hydrocodone Bitartrate and Acetaminophen, 71930-020 — Hydrocodone Bitartrate and Acetaminophen, 71930-021 — Hydrocodone Bitartrate and Acetaminophen, 71930-027 — Hydrocodone Bitartrate and Acetaminophen, 71930-042 — hydrocodone bitartrate and acetaminophen, 71930-043 — hydrocodone bitartrate and 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.