NDC 48201-001 – Sanaflu Xtra

Dextromethorphan Hydrobromide 10 mg/1; Phenylephrine Hydrochloride 5 mg/1; Acetaminophen 250 mg/1; Chlorpheniramine Maleate 2 mg/1 · Capsule, Gelatin Coated · Oral

Human Otc Drug

Product NDC48201-001

Product details

Brand name
Sanaflu Xtra
Generic name
Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Labeler
GRANDALL DISTRIBUTING, LLC
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
OTC MONOGRAPH DRUG · M013
Marketed since
April 30, 2015
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Sanaflu Xtra →

Package NDC codes (1)

Package NDCDescriptionSince
48201-001-1212 CAPSULE, GELATIN COATED in 1 BOX (48201-001-12)Apr 30, 2015