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berkley and jensen mucus relief

NDC 68391-000 · BJWC

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

68391-000-45 — 4 BLISTER PACK in 1 CARTON (68391-000-45) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68163-743 — Guaifenesin, 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, 68391-299 — Dextromethorphan HBr, Guaifenesin, 68391-711 — Dextromethorphan HBr, Guaifenesin, 68391-724 — Guaifenesin, 68391-812 — dextromethorphan HBr, guaifenesin, 68436-120 — Sorbutuss, 68788-8268 — dextromethorphan hydrobromide, guaifenesin, 68788-8300 — dextromethorphan hydrobromide, guaifenesin, 68788-8303 — dextromethorphan hydrobromide, guaifenesin, 68788-8361 — Guaifenesin and Codeine Phosphate, 68998-114 — Dextromethorphan Hydrobromide / 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.