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"0093-0083-98" National Drug Code (NDC)
Amlodipine Besylate 90 TABLET in 1 BOTTLE (0093-0083-98)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0083-98
Package Description
90 TABLET in 1 BOTTLE (0093-0083-98)
Product NDC
0093-0083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070710
End Marketing Date
20190630
Marketing Category Name
ANDA
Application Number
ANDA076846
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
2.5
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/0093-0083-98