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"61919-219-30" National Drug Code (NDC)
Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE (61919-219-30)
(Direct_Rx)
NDC Code
61919-219-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (61919-219-30)
Product NDC
61919-219
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190726
Marketing Category Name
ANDA
Application Number
ANDA078332
Manufacturer
Direct_Rx
Substance Name
CARVEDILOL
Strength
3.125
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/61919-219-30