Carvedilol - 0904-6096-61 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 0904-6096
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 12.5    mg/1 & nbsp;   Carvedilol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carvedilol

Product NDC: 0904-6096
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078251
Marketing Category: ANDA
Start Marketing Date: 20100618

Package Information of Carvedilol

Package NDC: 0904-6096-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-6096-61)

NDC Information of Carvedilol

NDC Code 0904-6096-61
Proprietary Name Carvedilol
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-6096-61)
Product NDC 0904-6096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100618
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name CARVEDILOL
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]

Complete Information of Carvedilol


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