NDC 58602-864 – Guaifenesin

Guaifenesin 600 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC58602-864

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Aurohealth LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210453
Marketed since
March 11, 2021
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
58602-864-985 BLISTER PACK in 1 CARTON (58602-864-98) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 11, 2021

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