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sunmark fexofenadine hydrochloride
sunmark fexofenadine hydrochloride - 49348-968-57 - (fexofenadine hydrochloride)
Drug Information of sunmark fexofenadine hydrochloride
| Product NDC: | 49348-968 |
| Proprietary Name: | sunmark fexofenadine hydrochloride |
| Non Proprietary Name: | fexofenadine hydrochloride |
| Active Ingredient(s): | 180 mg/1 & nbsp; fexofenadine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark fexofenadine hydrochloride
| Product NDC: | 49348-968 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110414 |
Package Information of sunmark fexofenadine hydrochloride
| Package NDC: | 49348-968-57 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (49348-968-57) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of sunmark fexofenadine hydrochloride
| NDC Code | 49348-968-57 |
| Proprietary Name | sunmark fexofenadine hydrochloride |
| Package Description | 3 BLISTER PACK in 1 CARTON (49348-968-57) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 49348-968 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110414 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
