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"0480-0083-05" National Drug Code (NDC)
Amlodipine Besylate 500 TABLET in 1 BOTTLE (0480-0083-05)
(Teva Pharmaceuticals, Inc.)
NDC Code
0480-0083-05
Package Description
500 TABLET in 1 BOTTLE (0480-0083-05)
Product NDC
0480-0083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20221001
Marketing Category Name
ANDA
Application Number
ANDA076846
Manufacturer
Teva Pharmaceuticals, Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0480-0083-05