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Allegra--D 24 Hour
Allegra--D 24 Hour - 54868-5419-0 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)
Drug Information of Allegra--D 24 Hour
| Product NDC: | 54868-5419 |
| Proprietary Name: | Allegra--D 24 Hour |
| Non Proprietary Name: | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 180; 240 mg/1; mg/1 & nbsp; fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allegra--D 24 Hour
| Product NDC: | 54868-5419 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021704 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050914 |
Package Information of Allegra--D 24 Hour
| Package NDC: | 54868-5419-0 |
| Package Description: | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5419-0) |
NDC Information of Allegra--D 24 Hour
| NDC Code | 54868-5419-0 |
| Proprietary Name | Allegra--D 24 Hour |
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5419-0) |
| Product NDC | 54868-5419 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20050914 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 180; 240 |
| 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] |
