Skip to main content

Guaifenesin 1200 mg

NDC 70677-1258 · Strategic Sourcing Services, LLC

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

70677-1258-1 — 1 BLISTER PACK in 1 CARTON (70677-1258-1) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-1050 — Guaifenesin, Dextromethorphan HBr, 70677-1051 — Guaifenesin, 70677-1052 — Guaifenesin, 70677-1054 — Guaifenesin, 70677-1055 — Dextromethorphan Hydrobromide / Guaifenesin, 70677-1056 — Guaifenesin/phenylephrine, 70677-1185 — Dextromethorphan HBr, Guaifenesin, 70677-1186 — Guaifenesin, 70677-1187 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 70677-1257 — Guaifenesin, 70677-1259 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 70677-1261 — Dextromethorphan HBr Guaifenesin, 70677-1263 — Guaifenesin and Pseudoephedrine HCl, 70677-1272 — guaifenesin and pseudoephedrine hydrochloride, 70677-1273 — guaifenesin, pseudoephedrine hydrochloride, 70677-1291 — guaifenesin, 70692-181 — Dextromethorphan Hydrobromide, Guaifenesin, 70692-836 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 71179-002 — Guaifenesin, 71179-011 — Guaifenesin and 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.