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Guaifenesin Extended Release 1200 mg

NDC 49483-724 · TIME CAP LABORATORIES, INC.

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

Packages

49483-724-70 — 70 TABLET in 1 BOTTLE (49483-724-70)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49035-930 — Dextromethorphan HBr, Guaifenesin, 49035-956 — Guaifenesin and Dextromethorphan HBr, 49035-960 — Guaifenesin and Dextromethorphan HBr, 49035-976 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 49348-728 — Dextromethorphan Hydrobromide / Guaifenesin, 49348-729 — Guaifenesin, 49348-774 — Guaifenesin/phenylephrine, 49483-272 — GUAIFENESIN, 49483-280 — GUAIFENESIN DEXTROMETHORPHAN, 49483-723 — Guaifenesin, 49580-0385 — Dextromethorphan HBr, Guaifenesin, 49580-0415 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 49580-0834 — Dextromethorphan HBr Guaifenesin, 49873-302 — dextromethorphan hydrobromide, guaifenesin, 49873-306 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 50066-301 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 50066-308 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 50066-313 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 50066-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 50066-505 — Dextromethorphan Hydrobromide and 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.