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"70518-0095-2" National Drug Code (NDC)
Carvedilol 180 TABLET, FILM COATED in 1 BOTTLE (70518-0095-2)
(REMEDYREPACK INC.)
NDC Code
70518-0095-2
Package Description
180 TABLET, FILM COATED in 1 BOTTLE (70518-0095-2)
Product NDC
70518-0095
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20161229
Marketing Category Name
ANDA
Application Number
ANDA078251
Manufacturer
REMEDYREPACK INC.
Substance Name
CARVEDILOL
Strength
12.5
Strength Unit
mg/1
Pharmacy Classes
Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0095-2