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DRx Choice

NDC 68163-743 · Raritan Pharmaceuticals Inc

Generic nameGuaifenesin
Dosage formSYRUP
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength200 mg/10mL
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

68163-743-04 — 1 BOTTLE in 1 CARTON (68163-743-04) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68163-747 — Dextromethorphan HBr and Guaifenesin, 68163-748 — Guaifenesin and Phenylephrine Hcl, 68196-033 — Guaifenesin, 68196-405 — Guaifenesin, 68196-812 — dextromethorphan HBr, guaifenesin, 68196-960 — GUAIFENESIN, 68196-996 — Guaifenesin, 68196-999 — Guaifenesin and Dextromethorphan HBR, 68210-4158 — GUAIFENESIN, 68391-000 — 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.