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Montelukast
Montelukast - 0781-5560-92 - (Montelukast)
Drug Information of Montelukast
| Product NDC: | 0781-5560 |
| Proprietary Name: | Montelukast |
| Non Proprietary Name: | Montelukast |
| Active Ingredient(s): | 10 mg/1 & nbsp; Montelukast |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Montelukast
| Product NDC: | 0781-5560 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200889 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120803 |
Package Information of Montelukast
| Package NDC: | 0781-5560-92 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (0781-5560-92) |
NDC Information of Montelukast
| NDC Code | 0781-5560-92 |
| Proprietary Name | Montelukast |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0781-5560-92) |
| Product NDC | 0781-5560 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Montelukast |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120803 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | MONTELUKAST SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA] |
