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Fexofenadine Hydrochloride - 21695-462-10 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 21695-462
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine Hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   Fexofenadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fexofenadine Hydrochloride

Product NDC: 21695-462
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of Fexofenadine Hydrochloride

Package NDC: 21695-462-10
Package Description: 10 TABLET in 1 BOTTLE (21695-462-10)

NDC Information of Fexofenadine Hydrochloride

NDC Code 21695-462-10
Proprietary Name Fexofenadine Hydrochloride
Package Description 10 TABLET in 1 BOTTLE (21695-462-10)
Product NDC 21695-462
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fexofenadine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091209
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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