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mucus relief

NDC 41250-654 · Meijer Distribution Inc

Generic nameguaifenesin
Dosage formTABLET, MULTILAYER, 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

41250-654-02 — 3 BLISTER PACK in 1 CARTON (41250-654-02) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

41250-654-74 — 1 BLISTER PACK in 1 CARTON (41250-654-74) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-219 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-261 — Dextromethorphan HBr, Guaifenesin, 41250-275 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-436 — dextromethorphan hydrobromide, guaifenesin, 41250-446 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 41250-533 — Dextromethorphan HBr and Guaifenesin, 41250-547 — Guaifenesin, Pseudoephedrine HCl, 41250-574 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 41250-643 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 41250-663 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-684 — Guaifenesin, 41250-713 — Guaifenesin, 41250-748 — Dextromethorphan HBr and Guaifenesin, 41250-776 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 41250-812 — dextromethorphan HBr, guaifenesin, 41250-979 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-981 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41415-994 — Guaifenesin and Pseudoephedrine Hydrochloride, 41415-996 — 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.