NDC 0904-6808 – Montelukast Sodium

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

Human Prescription Drug

Product NDC0904-6808

Product details

Brand name
Montelukast Sodium
Generic name
Montelukast Sodium
Labeler
Major Pharmaceuticals
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 (2)

Package NDCDescriptionSince
0904-6808-0650 BLISTER PACK in 1 CARTON (0904-6808-06) / 1 TABLET, FILM COATED in 1 BLISTER PACKSep 10, 2014
0904-6808-61100 BLISTER PACK in 1 CARTON (0904-6808-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKSep 10, 2014

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