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"68180-761-03" National Drug Code (NDC)
Nadolol 1000 TABLET in 1 BOTTLE (68180-761-03)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-761-03
Package Description
1000 TABLET in 1 BOTTLE (68180-761-03)
Product NDC
68180-761
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nadolol
Non-Proprietary Name
Nadolol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20171005
Marketing Category Name
ANDA
Application Number
ANDA209309
Manufacturer
Lupin Pharmaceuticals, Inc.
Substance Name
NADOLOL
Strength
20
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/68180-761-03