NDC 81033-102 – Guaifenesin

Guaifenesin 100 mg/5mL · Liquid · Oral

Human Otc Drug

Product NDC81033-102

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
KESIN PHARMA CORPORATION
Dosage form
Liquid
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
November 20, 2023
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (3)

Package NDCDescriptionSince
81033-102-16473 mL in 1 BOTTLE (81033-102-16)Apr 1, 2025
81033-102-5150 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05)Nov 20, 2023
81033-102-5250 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10)Nov 20, 2023

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