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Allergy relief - 59779-425-53 - (Fexofenadine HCl)

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Drug Information of Allergy relief

Product NDC: 59779-425
Proprietary Name: Allergy relief
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 Allergy relief

Product NDC: 59779-425
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076447
Marketing Category: ANDA
Start Marketing Date: 20110831

Package Information of Allergy relief

Package NDC: 59779-425-53
Package Description: 2 BLISTER PACK in 1 CARTON (59779-425-53) > 6 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Allergy relief

NDC Code 59779-425-53
Proprietary Name Allergy relief
Package Description 2 BLISTER PACK in 1 CARTON (59779-425-53) > 6 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 59779-425
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110831
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Allergy relief


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