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Fexofenadine
Fexofenadine - 55648-987-11 - (Fexofenadine)
Drug Information of Fexofenadine
| Product NDC: | 55648-987 |
| Proprietary Name: | Fexofenadine |
| Non Proprietary Name: | Fexofenadine |
| Active Ingredient(s): | 180 mg/1 & nbsp; Fexofenadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine
| Product NDC: | 55648-987 |
| Labeler Name: | Wockhardt Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120208 |
Package Information of Fexofenadine
| Package NDC: | 55648-987-11 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (55648-987-11) > 5 TABLET, FILM COATED in 1 BLISTER PACK (55648-987-09) |
NDC Information of Fexofenadine
| NDC Code | 55648-987-11 |
| Proprietary Name | Fexofenadine |
| Package Description | 3 BLISTER PACK in 1 CARTON (55648-987-11) > 5 TABLET, FILM COATED in 1 BLISTER PACK (55648-987-09) |
| Product NDC | 55648-987 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fexofenadine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120208 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt Limited |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
