NDC 63629-7115 – Mucinex

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

Human Otc Drug

Product NDC63629-7115

Product details

Brand name
Mucinex
Generic name
Guaifenesin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA · NDA021282
Marketed since
July 3, 2012
Listing expires
December 31, 2027
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Mucinex →

Package NDC codes (7)

Package NDCDescriptionSince
63629-7115-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-1)Apr 2, 2024
63629-7115-220 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-2)Oct 17, 2016
63629-7115-360 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-3)Apr 2, 2024
63629-7115-440 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-4)Feb 4, 2019
63629-7115-514 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-5)Apr 2, 2024
63629-7115-66 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-6)Apr 2, 2024
63629-7115-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7115-7)Apr 2, 2024

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