Carvedilol - 49349-870-02 - (Carvedilol)

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Drug Information of Carvedilol

Product NDC: 49349-870
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: 49349-870
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078332
Marketing Category: ANDA
Start Marketing Date: 20120117

Package Information of Carvedilol

Package NDC: 49349-870-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-870-02)

NDC Information of Carvedilol

NDC Code 49349-870-02
Proprietary Name Carvedilol
Package Description 30 TABLET in 1 BLISTER PACK (49349-870-02)
Product NDC 49349-870
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carvedilol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120117
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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


General Information