NDC 31722-726 – Montelukast Sodium
Montelukast Sodium 10 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-726
Product details
- Brand name
- Montelukast Sodium
- Generic name
- Montelukast Sodium
- Labeler
- Camber Pharmaceuticals, Inc.
- 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
Uses, dosage, side effects and warnings for Montelukast Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-726-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-726-01) | Sep 10, 2014 |
| 31722-726-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-726-10) | Sep 10, 2014 |
| 31722-726-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-726-30) | Sep 10, 2014 |
| 31722-726-32 | 10 BLISTER PACK in 1 CARTON (31722-726-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-726-31) | Sep 10, 2014 |
| 31722-726-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-726-90) | Sep 10, 2014 |
Recalls mentioning this NDC
- D-1213-2018 Oct 3, 2018 · Class II
Discoloration: A complaint was received from a pharmacist for the presence of blue specks on tablets. - D-0081-2019 Oct 3, 2018 · Class I
Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg tablets may contain 90 tablets of Losartan Potassium 50 mg. - D-0623-2017 Apr 5, 2017 · Class III
Discoloration: the firm received a complaint of a sealed bottle in which tablets inside had blue spots and a blue powder inside the bottle.
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