NDC 51316-071 – Guaifenesin

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

Human Otc Drug

Product NDC51316-071

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
CVS
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209254
Marketed since
October 7, 2022
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
51316-071-681 BLISTER PACK in 1 CARTON (51316-071-68) / 68 TABLET, EXTENDED RELEASE in 1 BLISTER PACKOct 7, 2022

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