NDC 71309-461 – Guaifenesin

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

Human Otc Drug

Product NDC71309-461

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Safrel Pharmaceuticals, 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
71309-461-5656 TABLET, EXTENDED RELEASE in 1 BOTTLE (71309-461-56)Jun 29, 2022

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