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"69097-869-15" National Drug Code (NDC)
Nadolol 1000 TABLET in 1 BOTTLE (69097-869-15)
(Cipla USA Inc.)
NDC Code
69097-869-15
Package Description
1000 TABLET in 1 BOTTLE (69097-869-15)
Product NDC
69097-869
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nadolol
Non-Proprietary Name
Nadolol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160223
Marketing Category Name
ANDA
Application Number
ANDA203455
Manufacturer
Cipla USA Inc.
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/69097-869-15