Entacapone - 55648-711-04 - (Entacapone)

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Drug Information of Entacapone

Product NDC: 55648-711
Proprietary Name: Entacapone
Non Proprietary Name: Entacapone
Active Ingredient(s): 200    mg/1 & nbsp;   Entacapone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Entacapone

Product NDC: 55648-711
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078941
Marketing Category: ANDA
Start Marketing Date: 20120816

Package Information of Entacapone

Package NDC: 55648-711-04
Package Description: 10 BLISTER PACK in 1 CARTON (55648-711-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Entacapone

NDC Code 55648-711-04
Proprietary Name Entacapone
Package Description 10 BLISTER PACK in 1 CARTON (55648-711-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55648-711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Entacapone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120816
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name ENTACAPONE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC]

Complete Information of Entacapone


General Information