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Mucinex

NDC 68084-572 · American Health Packaging

Generic nameGuaifenesin
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength600 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryNDA

Packages

68084-572-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-572-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-572-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67544-149 — Guaifenesin, 67751-171 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 68001-561 — Guaifenesin, 68016-674 — Guaifenesin, Dextromethorphan HBr, 68016-740 — Dextromethorphan HBr, Guaifenesin, 68016-744 — Dextromethorphan HBr, Guaifenesin, 68071-3938 — Dextromethorphan HBr, Guaifenesin, 68071-5173 — Codeine Phosphate and Guaifenesin, 68094-048 — Guaifenesin, 68163-605 — Dextromethorphan Hydrobromide and Guaifenesin, 68163-737 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 68163-738 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 68163-743 — Guaifenesin, 68163-747 — Dextromethorphan HBr and Guaifenesin, 68163-748 — Guaifenesin and Phenylephrine Hcl, 68196-033 — Guaifenesin, 68196-405 — Guaifenesin, 68196-812 — dextromethorphan HBr, guaifenesin, +1437 more

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