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Guaifenesin

NDC 68001-561 · BluePoint Laboratories

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

68001-561-17 — 8 BLISTER PACK in 1 CARTON (68001-561-17) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67091-470 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 67091-691 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 67296-1467 — Guaifenesin, 67296-2223 — guaifenesin, 67414-402 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 67414-507 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 67544-149 — Guaifenesin, 67751-171 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 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, 68084-572 — 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, +1437 more

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