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Guaifenesin

NDC 69848-017 · GRANULES USA, INC.

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

69848-017-02 — 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-903 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-904 — Dextromethorphan Hydrobromide Guaifenesin, 69842-926 — Dextromethorphan HBr, Guaifenesin, 69842-933 — Guaifenesin, Dextromethorphan HBr, 69842-937 — Dextromethorphan HBr and Guaifenesin, 69842-942 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-963 — guaifenesin, dextromethorphan hydrobromide, 69842-969 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL, 69842-996 — Dextromethorphan Hydrobromide / Guaifenesin, 69842-997 — Guaifenesin/phenylephrine, 69848-018 — Guaifenesin, 70000-0055 — Guaifenesin, 70000-0056 — Dextromethorphan Hydrobromide / Guaifenesin, 70000-0080 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70000-0083 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 70000-0133 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 70000-0141 — Guaifenesin, Phenylephrine HCl, 70000-0192 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 70000-0278 — Dextromethorphan HBr and Guaifenesin, 70000-0464 — Guaifenesin, Dextromethorphan HBr, +1437 more

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