MONTELUKAST SODIUM
- Product NDC
- 71335-0629
- 11-digit product format
- 713350629
- Labeler code
- 71335
- Product ID
- 71335-0629_eb08cffe-93b0-43cd-97ea-81608c6dc4c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MONTELUKAST
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203328
- Marketing category
- ANDA
- Marketing start
- 2015-08-13
- Marketing end
- 0000-00-00
- Substance
- MONTELUKAST SODIUM
- Active strength
- 5 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0629-1 | 71335062901 | 30 TABLET, CHEWABLE in 1 BOTTLE (71335-0629-1) | 2016-09-20 | 0000-00-00 | No | No | Current |
| 71335-0629-2 | 71335062902 | 90 TABLET, CHEWABLE in 1 BOTTLE (71335-0629-2) | 2016-09-20 | 0000-00-00 | No | No | Current |
| 71335-0629-3 | 71335062903 | 60 TABLET, CHEWABLE in 1 BOTTLE (71335-0629-3) | 2016-09-20 | 0000-00-00 | No | No | Current |
| 71335-0629-4 | 71335062904 | 28 TABLET, CHEWABLE in 1 BOTTLE (71335-0629-4) | 2016-09-20 | 0000-00-00 | No | No | Current |