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"69097-837-15" National Drug Code (NDC)
Amlodipine Besylate 1000 TABLET in 1 BOTTLE (69097-837-15)
(Cipla USA Inc.)
NDC Code
69097-837-15
Package Description
1000 TABLET in 1 BOTTLE (69097-837-15)
Product NDC
69097-837
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160701
Marketing Category Name
ANDA
Application Number
ANDA077955
Manufacturer
Cipla USA Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-837-15