NDC 71335-9616 – Guaifenesin

Guaifenesin 400 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71335-9616

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
August 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9616-130 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)Apr 3, 2024
71335-9616-220 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2)Dec 28, 2022
71335-9616-350 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3)Apr 3, 2024
71335-9616-460 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4)Apr 3, 2024
71335-9616-540 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)Apr 3, 2024

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