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Guaifenesin

NDC 58602-864 · Aurohealth LLC

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 categoryANDA

Packages

58602-864-98 — 5 BLISTER PACK in 1 CARTON (58602-864-98) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58602-715 — Guaifenesin and Dextromethorphan HBr, 58602-810 — Guaifenesin, 58602-811 — Guaifenesin, 58602-824 — Guaifenesin and Dextromethorphan HBr, 58602-825 — Guaifenesin and Dextromethorphan HBr, 58602-833 — Guaifenesin and Pseudoephedrine HCl, 58602-834 — Guaifenesin and Pseudoephedrine HCl, 58602-849 — Guaifenesin and Dextromethorphan HBr, 58602-853 — Guaifenesin, 58602-857 — Guaifenesin, 58602-865 — Guaifenesin, 58602-871 — Guaifenesin and Dextromethorphan HBr, 58657-500 — Codeine Phosphate and Guaifenesin, 58657-504 — Guaifenesin and Dextromethorphan Hydrobromide, 58657-505 — Guaifenesin and Dextromethorphan Hydrobromide, 58657-508 — Guaifenesin, 58657-509 — Guaifenesin, 58809-187 — Dextromethorphan HBr, Guaifenesin, 58809-217 — Choline Salicylate, Dextromethorphan Hydrobromide, Guaifenesin, 58809-218 — Choline Salicylate,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.