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SINGULAIR
SINGULAIR - 21695-221-30 - (montelukast sodium)
Drug Information of SINGULAIR
| Product NDC: | 21695-221 |
| Proprietary Name: | SINGULAIR |
| Non Proprietary Name: | montelukast sodium |
| Active Ingredient(s): | 10 mg/1 & nbsp; montelukast sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SINGULAIR
| Product NDC: | 21695-221 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020829 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980220 |
Package Information of SINGULAIR
| Package NDC: | 21695-221-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (21695-221-30) |
NDC Information of SINGULAIR
| NDC Code | 21695-221-30 |
| Proprietary Name | SINGULAIR |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (21695-221-30) |
| Product NDC | 21695-221 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | montelukast sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980220 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MONTELUKAST SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA] |
