NDC 58602-857 – Guaifenesin

Guaifenesin 1200 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC58602-857

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Aurohealth LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210453
Marketed since
July 3, 2026
Listing expires
December 31, 2027
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
58602-857-936 BLISTER PACK in 1 CARTON (58602-857-93) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJul 3, 2026

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