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Flecainide Acetate - 54868-5074-3 - (Flecainide Acetate)

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Drug Information of Flecainide Acetate

Product NDC: 54868-5074
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: 54868-5074
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076278
Marketing Category: ANDA
Start Marketing Date: 20040630

Package Information of Flecainide Acetate

Package NDC: 54868-5074-3
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-5074-3)

NDC Information of Flecainide Acetate

NDC Code 54868-5074-3
Proprietary Name Flecainide Acetate
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-5074-3)
Product NDC 54868-5074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flecainide Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040630
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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