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Flecainide Acetate - 0555-0859-02 - (Flecainide Acetate)

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Drug Information of Flecainide Acetate

Product NDC: 0555-0859
Proprietary Name: Flecainide Acetate
Non Proprietary Name: Flecainide Acetate
Active Ingredient(s): 50    mg/1 & nbsp;   Flecainide Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Flecainide Acetate

Product NDC: 0555-0859
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075882
Marketing Category: ANDA
Start Marketing Date: 20021118

Package Information of Flecainide Acetate

Package NDC: 0555-0859-02
Package Description: 100 TABLET in 1 BOTTLE (0555-0859-02)

NDC Information of Flecainide Acetate

NDC Code 0555-0859-02
Proprietary Name Flecainide Acetate
Package Description 100 TABLET in 1 BOTTLE (0555-0859-02)
Product NDC 0555-0859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flecainide Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021118
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name FLECAINIDE ACETATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Flecainide Acetate


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