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FEXOFENADINE HYDROCHLORIDE
FEXOFENADINE HYDROCHLORIDE - 62756-543-16 - (FEXOFENADINE HYDROCHLORIDE)
Drug Information of FEXOFENADINE HYDROCHLORIDE
| Product NDC: | 62756-543 |
| Proprietary Name: | FEXOFENADINE HYDROCHLORIDE |
| Non Proprietary Name: | FEXOFENADINE HYDROCHLORIDE |
| Active Ingredient(s): | 60 mg/1 & nbsp; FEXOFENADINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FEXOFENADINE HYDROCHLORIDE
| Product NDC: | 62756-543 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091567 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120206 |
Package Information of FEXOFENADINE HYDROCHLORIDE
| Package NDC: | 62756-543-16 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (62756-543-16) |
NDC Information of FEXOFENADINE HYDROCHLORIDE
| NDC Code | 62756-543-16 |
| Proprietary Name | FEXOFENADINE HYDROCHLORIDE |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (62756-543-16) |
| Product NDC | 62756-543 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | FEXOFENADINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120206 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
