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"70518-0356-0" National Drug Code (NDC)
Carvedilol 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0356-0)
(REMEDYREPACK INC.)
NDC Code
70518-0356-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0356-0)
Product NDC
70518-0356
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20170323
Marketing Category Name
ANDA
Application Number
ANDA077614
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/70518-0356-0