NDC 71335-1979 – Montelukast
Montelukast Sodium 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1979
Product details
- Brand name
- Montelukast
- Generic name
- Montelukast
- Labeler
- Bryant Ranch Prepack
- 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
- Montelukast Sodium 10 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1979-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1979-1) | Dec 21, 2021 |
| 71335-1979-2 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-1979-2) | Dec 21, 2021 |
| 71335-1979-3 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1979-3) | Dec 21, 2021 |
| 71335-1979-4 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1979-4) | Dec 21, 2021 |
| 71335-1979-5 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1979-5) | Dec 21, 2021 |
| 71335-1979-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1979-6) | Oct 27, 2021 |
| 71335-1979-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1979-7) | Dec 21, 2021 |
| 71335-1979-8 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1979-8) | Dec 21, 2021 |
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