Carvedilol - 0904-6098-61 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 0904-6098
Proprietary Name: Carvedilol
Non Proprietary Name: Carvedilol
Active Ingredient(s): 3.125    mg/1 & nbsp;   Carvedilol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carvedilol

Product NDC: 0904-6098
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078251
Marketing Category: ANDA
Start Marketing Date: 20100607

Package Information of Carvedilol

Package NDC: 0904-6098-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-6098-61)

NDC Information of Carvedilol

NDC Code 0904-6098-61
Proprietary Name Carvedilol
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-6098-61)
Product NDC 0904-6098
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100607
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name CARVEDILOL
Strength Number 3.125
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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