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Flecainide Acetate - 63304-796-01 - (Flecainide)

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Drug Information of Flecainide Acetate

Product NDC: 63304-796
Proprietary Name: Flecainide Acetate
Non Proprietary Name: Flecainide
Active Ingredient(s): 150    mg/1 & nbsp;   Flecainide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Flecainide Acetate

Product NDC: 63304-796
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076421
Marketing Category: ANDA
Start Marketing Date: 20040228

Package Information of Flecainide Acetate

Package NDC: 63304-796-01
Package Description: 100 TABLET in 1 BOTTLE, UNIT-DOSE (63304-796-01)

NDC Information of Flecainide Acetate

NDC Code 63304-796-01
Proprietary Name Flecainide Acetate
Package Description 100 TABLET in 1 BOTTLE, UNIT-DOSE (63304-796-01)
Product NDC 63304-796
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flecainide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040228
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name FLECAINIDE ACETATE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Flecainide Acetate


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