NDC 58602-849 – Guaifenesin and Dextromethorphan HBr

Guaifenesin 1200 mg/1; Dextromethorphan Hydrobromide 60 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC58602-849

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
May 16, 2020
Listing expires
December 31, 2027
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 (5)

Package NDCDescriptionSince
58602-849-118 BLISTER PACK in 1 CARTON (58602-849-11) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACKAug 13, 2020
58602-849-151 BOTTLE in 1 CARTON (58602-849-15) / 60 TABLET, EXTENDED RELEASE in 1 BOTTLEAug 13, 2020
58602-849-571 BOTTLE in 1 CARTON (58602-849-57) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLESep 8, 2020
58602-849-641 BLISTER PACK in 1 CARTON (58602-849-64) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 24, 2021
58602-849-652 BLISTER PACK in 1 CARTON (58602-849-65) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMay 16, 2020

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