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Fexofenadine Hydrochloride - 52125-570-20 - (Fexofenadine HCl)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 52125-570
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine HCl
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 52125-570
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079112
Marketing Category: ANDA
Start Marketing Date: 20130523

Package Information of Fexofenadine Hydrochloride

Package NDC: 52125-570-20
Package Description: 100 TABLET in 1 VIAL (52125-570-20)

NDC Information of Fexofenadine Hydrochloride

NDC Code 52125-570-20
Proprietary Name Fexofenadine Hydrochloride
Package Description 100 TABLET in 1 VIAL (52125-570-20)
Product NDC 52125-570
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Fexofenadine Hydrochloride


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