NDC 52083-655 – G-Supress DX

Dextromethorphan Hydrobromide 5 mg/mL; Guaifenesin 50 mg/mL; Phenylephrine Hydrochloride 2.5 mg/mL · Syrup · Oral

Human Otc Drug 1 recall

Product NDC52083-655

Product details

Brand name
G-Supress DX
Generic name
Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Labeler
KRAMER NOVIS
Dosage form
Syrup
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M012
Marketed since
March 29, 2011
Listing expires
December 31, 2026
Pharmacologic class
Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for G-Supress DX →

Package NDC codes (1)

Package NDCDescriptionSince
52083-655-0130 mL in 1 BOTTLE (52083-655-01)Mar 29, 2011

Recalls mentioning this NDC