NDC 31722-726 – Montelukast Sodium

Montelukast Sodium 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 3 recalls

Product NDC31722-726

Product details

Brand name
Montelukast Sodium
Generic name
Montelukast Sodium
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
September 10, 2014
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast Sodium →

Package NDC codes (5)

Package NDCDescriptionSince
31722-726-01100 TABLET, FILM COATED in 1 BOTTLE (31722-726-01)Sep 10, 2014
31722-726-101000 TABLET, FILM COATED in 1 BOTTLE (31722-726-10)Sep 10, 2014
31722-726-3030 TABLET, FILM COATED in 1 BOTTLE (31722-726-30)Sep 10, 2014
31722-726-3210 BLISTER PACK in 1 CARTON (31722-726-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-726-31)Sep 10, 2014
31722-726-9090 TABLET, FILM COATED in 1 BOTTLE (31722-726-90)Sep 10, 2014

Recalls mentioning this NDC

Other Montelukast Sodium products