NDC 55111-725 – Montelukast Sodium

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

Human Prescription Drug 1 recall

Product NDC55111-725

Product details

Brand name
Montelukast Sodium
Generic name
Montelukast Sodium
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA201582
Marketed since
August 6, 2012
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
55111-725-01100 TABLET, COATED in 1 BOTTLE (55111-725-01)Aug 6, 2012
55111-725-101000 TABLET, COATED in 1 BOTTLE (55111-725-10)Aug 6, 2012
55111-725-3030 TABLET, COATED in 1 BOTTLE (55111-725-30)Aug 6, 2012
55111-725-7810 BLISTER PACK in 1 CARTON (55111-725-78) / 10 TABLET, COATED in 1 BLISTER PACK (55111-725-79)Aug 6, 2012
55111-725-9090 TABLET, COATED in 1 BOTTLE (55111-725-90)Aug 6, 2012

Recalls mentioning this NDC

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