NDC 58602-871 – Guaifenesin and Dextromethorphan HBr

Guaifenesin 600 mg/1; Dextromethorphan Hydrobromide 30 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC58602-871

Product details

Brand name
Guaifenesin and Dextromethorphan HBr
Generic name
Guaifenesin and Dextromethorphan HBr
Labeler
Aurohealth LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206941
Marketed since
February 24, 2021
Listing expires
December 31, 2026
Pharmacologic class
Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin and Dextromethorphan HBr →

Package NDC codes (1)

Package NDCDescriptionSince
58602-871-831 BLISTER PACK in 1 CARTON (58602-871-83) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 24, 2021

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