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Sunmark fexofenadine hydrochloride
Sunmark fexofenadine hydrochloride - 49348-970-02 - (Fexofenadine HCl)
Drug Information of Sunmark fexofenadine hydrochloride
| Product NDC: | 49348-970 |
| Proprietary Name: | Sunmark fexofenadine hydrochloride |
| Non Proprietary Name: | Fexofenadine HCl |
| Active Ingredient(s): | 60 mg/1 & nbsp; Fexofenadine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark fexofenadine hydrochloride
| Product NDC: | 49348-970 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110906 |
Package Information of Sunmark fexofenadine hydrochloride
| Package NDC: | 49348-970-02 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (49348-970-02) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Sunmark fexofenadine hydrochloride
| NDC Code | 49348-970-02 |
| Proprietary Name | Sunmark fexofenadine hydrochloride |
| Package Description | 2 BLISTER PACK in 1 CARTON (49348-970-02) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 49348-970 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fexofenadine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110906 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
