NDC 55111-725 – Montelukast Sodium
Montelukast Sodium 10 mg/1 · Tablet, Coated · Oral
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
- Montelukast Sodium 10 mg/1
Uses, dosage, side effects and warnings for Montelukast Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-725-01 | 100 TABLET, COATED in 1 BOTTLE (55111-725-01) | Aug 6, 2012 |
| 55111-725-10 | 1000 TABLET, COATED in 1 BOTTLE (55111-725-10) | Aug 6, 2012 |
| 55111-725-30 | 30 TABLET, COATED in 1 BOTTLE (55111-725-30) | Aug 6, 2012 |
| 55111-725-78 | 10 BLISTER PACK in 1 CARTON (55111-725-78) / 10 TABLET, COATED in 1 BLISTER PACK (55111-725-79) | Aug 6, 2012 |
| 55111-725-90 | 90 TABLET, COATED in 1 BOTTLE (55111-725-90) | Aug 6, 2012 |
Recalls mentioning this NDC
- D-0086-2024 Nov 15, 2023 · Class II
Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a bottle of Montelukast Sodium Tablets, USP 10mg, identified as metoprolol 25 mg.
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