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Mucinex

NDC 63629-7115 · Bryant Ranch Prepack

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

63629-7115-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-1)

63629-7115-2 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-2)

63629-7115-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-3)

63629-7115-4 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-4)

63629-7115-5 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-5)

63629-7115-6 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-6)

63629-7115-7 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63102-101 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl, 63102-102 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl, 63102-104 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63102-110 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 63102-120 — Dextromethorphan Hydrobromide, Guaifenesin, Pseudoephedrine Hydrochloride, 63102-130 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 63102-140 — Dextromethorphan Hydrobromide, Guaifenesin, 63187-954 — Guaifenesin, 63304-106 — Guaifenesin and Dextromethorphan HBr, 63304-110 — Guaifenesin and Dextromethorphan HBr, 63629-7886 — Guaifenesin, 63654-342 — Guaifensin, Dextromethorphan, 63739-067 — Guaifenesin, 63824-008 — Guaifenesin, 63824-015 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 63824-019 — dextromethorphan hydrobromide and guaifenesin, 63824-023 — Guaifenesin, 63824-041 — Guaifenesin and Pseudoephedrine Hydrochloride, 63824-056 — Guaifenesin and Dextromethorphan Hydrobromide, 63824-057 — Guaifenesin and Pseudoephedrine Hydrochloride, +1437 more

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