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Zafirlukast
Zafirlukast - 68084-059-21 - (Zafirlukast)
Drug Information of Zafirlukast
| Product NDC: | 68084-059 |
| Proprietary Name: | Zafirlukast |
| Non Proprietary Name: | Zafirlukast |
| Active Ingredient(s): | 20 mg/1 & nbsp; Zafirlukast |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zafirlukast
| Product NDC: | 68084-059 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090372 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130607 |
Package Information of Zafirlukast
| Package NDC: | 68084-059-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-059-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-059-11) |
NDC Information of Zafirlukast
| NDC Code | 68084-059-21 |
| Proprietary Name | Zafirlukast |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-059-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-059-11) |
| Product NDC | 68084-059 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zafirlukast |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130607 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | ZAFIRLUKAST |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA] |
