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Allegra-D
Allegra-D - 63629-1249-2 - (FEXOFENADINE AND PSEUDOEPHEDRINE)
Drug Information of Allegra-D
| Product NDC: | 63629-1249 |
| Proprietary Name: | Allegra-D |
| Non Proprietary Name: | FEXOFENADINE AND PSEUDOEPHEDRINE |
| Active Ingredient(s): | 60; 60 mg/1; mg/1 & nbsp; FEXOFENADINE AND PSEUDOEPHEDRINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allegra-D
| Product NDC: | 63629-1249 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA020786 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090304 |
Package Information of Allegra-D
| Package NDC: | 63629-1249-2 |
| Package Description: | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1249-2) |
NDC Information of Allegra-D
| NDC Code | 63629-1249-2 |
| Proprietary Name | Allegra-D |
| Package Description | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1249-2) |
| Product NDC | 63629-1249 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FEXOFENADINE AND PSEUDOEPHEDRINE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090304 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | FEXOFENADINE; PSEUDOEPHEDRINE |
| Strength Number | 60; 60 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
