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"59762-0812-1" National Drug Code (NDC)
Nadolol 100 TABLET in 1 BOTTLE (59762-0812-1)
(Greenstone LLC)
NDC Code
59762-0812-1
Package Description
100 TABLET in 1 BOTTLE (59762-0812-1)
Product NDC
59762-0812
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nadolol
Non-Proprietary Name
Nadolol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140428
End Marketing Date
20230831
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA018063
Manufacturer
Greenstone LLC
Substance Name
NADOLOL
Strength
80
Strength Unit
mg/1
Pharmacy Classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-0812-1