NDC 16103-379 – Guaifenesin

Guaifenesin 400 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC16103-379

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Pharbest Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
May 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (1)

Package NDCDescriptionSince
16103-379-041 BOTTLE, PLASTIC in 1 CARTON (16103-379-04) / 30 TABLET in 1 BOTTLE, PLASTICMay 1, 2018

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