NDC 71179-002 – Guaifenesin

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

Human Otc Drug

Product NDC71179-002

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
VESPYR BRANDS LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210453
Marketed since
June 27, 2022
Listing expires
December 31, 2027
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
71179-002-213 BLISTER PACK in 1 CARTON (71179-002-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 27, 2022

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