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Fexofenadine Hydrochloride - 49999-771-30 - (Fexofenadine Hydrochloride)

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Drug Information of Fexofenadine Hydrochloride

Product NDC: 49999-771
Proprietary Name: Fexofenadine Hydrochloride
Non Proprietary Name: Fexofenadine Hydrochloride
Active Ingredient(s): 60    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: 49999-771
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076502
Marketing Category: ANDA
Start Marketing Date: 20091209

Package Information of Fexofenadine Hydrochloride

Package NDC: 49999-771-30
Package Description: 30 TABLET in 1 BOTTLE (49999-771-30)

NDC Information of Fexofenadine Hydrochloride

NDC Code 49999-771-30
Proprietary Name Fexofenadine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (49999-771-30)
Product NDC 49999-771
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 Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name FEXOFENADINE HYDROCHLORIDE
Strength Number 60
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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