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"61919-533-30" National Drug Code (NDC)
Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE (61919-533-30)
(DIRECT RX)
NDC Code
61919-533-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (61919-533-30)
Product NDC
61919-533
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA078384
Manufacturer
DIRECT RX
Substance Name
CARVEDILOL
Strength
25
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/61919-533-30