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GUAIFENESIN

NDC 62207-569 · Granules India Ltd

Generic nameGUAIFENESIN
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength1200 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryANDA

Packages

62207-569-93 — 5 POUCH in 1 BOX (62207-569-93) / 2000 TABLET, EXTENDED RELEASE in 1 POUCH

62207-569-99 — 4200 TABLET, EXTENDED RELEASE in 1 BAG (62207-569-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60000-058 — Guaifenesin and Dextromethorphan HBr, 60687-817 — Guaifenesin and Dextromethorphan, 60687-828 — Guaifenesin and Dextromethorphan, 60687-852 — Guaifenesin, 60687-863 — Guaifenesin, 60687-874 — Guaifenesin, 61504-204 — Guaifenesin, 61787-515 — Dextromethorphan Hydrobromide and Guaifenesin, 62011-0060 — Guaifenesin, 62011-0475 — Guaifenesin and Pseudoephedrine Hydrochloride, 62207-570 — GUAIFENESIN, 62207-827 — Guaifenesin and Pseudoephedrine HCl, 62207-828 — Guaifenesin and Pseudoephedrine HCl, 62207-839 — GUAIFENESIN, 62207-840 — GUAIFENESIN, 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, +1437 more

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