NDC 42192-619 – Naproxen

Naproxen 125 mg/5mL · Suspension · Oral

Human Prescription Drug 1 recall

Product NDC42192-619

Product details

Brand name
Naproxen
Generic name
Naproxen
Labeler
Acella Pharmaceuticals, LLC
Dosage form
Suspension
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018965
Marketed since
November 12, 2020
Marketing end
January 31, 2028
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Naproxen →

Package NDC codes (1)

Package NDCDescriptionSince
42192-619-16473 mL in 1 BOTTLE (42192-619-16)Nov 12, 2020

Recalls mentioning this NDC

Other Naproxen products