NDC 71335-0514 – Montelukast Sodium
Montelukast Sodium 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0514
Product details
- Brand name
- Montelukast Sodium
- Generic name
- Montelukast Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202717
- Marketed since
- April 11, 2013
- 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 (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0514-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0514-1) | Mar 8, 2018 |
| 71335-0514-2 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-0514-2) | Dec 27, 2021 |
| 71335-0514-3 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0514-3) | Dec 27, 2021 |
| 71335-0514-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0514-4) | Aug 29, 2018 |
| 71335-0514-5 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0514-5) | Dec 27, 2021 |
| 71335-0514-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0514-6) | Feb 12, 2018 |
| 71335-0514-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0514-7) | Apr 12, 2019 |
| 71335-0514-8 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0514-8) | Dec 27, 2021 |
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