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"49349-870-02" National Drug Code (NDC)
Carvedilol 30 TABLET in 1 BLISTER PACK (49349-870-02)
(REMEDYREPACK INC.)
NDC Code
49349-870-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-870-02)
Product NDC
49349-870
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20120117
Marketing Category Name
ANDA
Application Number
ANDA078332
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/49349-870-02