Guaifenesin and Pseudoephedrine HCl

NDC 30142-137 · KROGER COMPANY

Generic nameGuaifenesin and Pseudoephedrine HCl

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE

Strength600; 60 mg/1; mg/1

Pharmacologic classAdrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC]

Marketing categoryANDA

Packages

30142-137-12 — 1 BLISTER PACK in 1 CARTON (30142-137-12) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

30142-137-17 — 2 BLISTER PACK in 1 CARTON (30142-137-17) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

25000-042 — Guaifenesin 600 mg, 27854-299 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 27854-350 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 28595-310 — DEXTROMETHORPHAN HBr, PSEUDOEPHEDRINE HCI, and TRIPROLIDINE HCI, 29300-313 — Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride, 29978-129 — Pseudoephedrine HCL, Pyrilamine Maleate, 29978-587 — Dextromethorphan Hydrobromide, Guaifenesin and Phenylephrine Hydrochloride, 29978-601 — Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride, 30142-059 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 30142-097 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 30142-275 — Guaifenesin and Dextromethorphan HBr, 30142-276 — Guaifenesin and Dextromethorphan HBr, 30142-423 — Ibuprofen and Pseudoephedrine Hydrochloride, 30142-447 — Fexofenadine HCl and Pseudoephedrine HCI, 30142-450 — cetirizine hydrochloride, pseudoephedrine hydrochloride, 30142-471 — Guaifenesin, 30142-472 — Dextromethorphan Hydrobromide / Guaifenesin, 30142-508 — Dextromethorphan Hydrobromide Guaifenesin, 30142-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 30142-611 — Fexofenadine HCl and Pseudoephedrine HCI, +1673 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.