Montelukast Sodium
- Product NDC
- 71335-0374
- 11-digit product format
- 713350374
- Labeler code
- 71335
- Product ID
- 71335-0374_666271bf-7405-4609-9573-266d911b6bbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Montelukast Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201515
- Marketing category
- ANDA
- Marketing start
- 2012-08-03
- Marketing end
- 0000-00-00
- Substance
- MONTELUKAST SODIUM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0374-1 | 71335037401 | 30 TABLET in 1 BOTTLE (71335-0374-1) | 30 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-2 | 71335037402 | 4 TABLET in 1 BOTTLE (71335-0374-2) | 4 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-3 | 71335037403 | 7 TABLET in 1 BOTTLE (71335-0374-3) | 7 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-4 | 71335037404 | 60 TABLET in 1 BOTTLE (71335-0374-4) | 60 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-5 | 71335037405 | 10 TABLET in 1 BOTTLE (71335-0374-5) | 10 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-6 | 71335037406 | 90 TABLET in 1 BOTTLE (71335-0374-6) | 90 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |
| 71335-0374-7 | 71335037407 | 120 TABLET in 1 BOTTLE (71335-0374-7) | 120 tablet | 2012-08-03 | 0000-00-00 | No | No | Current |