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Allegra D 12 Hour Allergy and Congestion
Allegra D 12 Hour Allergy and Congestion - 21695-931-20 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)
Drug Information of Allegra D 12 Hour Allergy and Congestion
| Product NDC: | 21695-931 |
| Proprietary Name: | Allegra D 12 Hour Allergy and Congestion |
| Non Proprietary Name: | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 60; 120 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 12 Hour Allergy and Congestion
| Product NDC: | 21695-931 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020786 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110303 |
Package Information of Allegra D 12 Hour Allergy and Congestion
| Package NDC: | 21695-931-20 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (21695-931-20) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Allegra D 12 Hour Allergy and Congestion
| NDC Code | 21695-931-20 |
| Proprietary Name | Allegra D 12 Hour Allergy and Congestion |
| Package Description | 4 BLISTER PACK in 1 CARTON (21695-931-20) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 21695-931 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110303 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 60; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
