NDC 70677-1257 – Guaifenesin 600 mg

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

Human Otc Drug

Product NDC70677-1257

Product details

Brand name
Guaifenesin 600 mg
Generic name
Guaifenesin
Labeler
Strategic Sourcing Services, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215932
Marketed since
March 15, 2022
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin 600 mg →

Package NDC codes (2)

Package NDCDescriptionSince
70677-1257-11 BLISTER PACK in 1 CARTON (70677-1257-1) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 15, 2025
70677-1257-22 BLISTER PACK in 1 CARTON (70677-1257-2) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 15, 2025

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