NDC 80513-413 – Guaifenesin

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

Human Otc Drug

Product NDC80513-413

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Advanced Rx LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213420
Marketed since
December 18, 2020
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
80513-413-11110 TABLET, EXTENDED RELEASE in 1 BOTTLE (80513-413-11)Jul 1, 2025

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