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"68382-121-05" National Drug Code (NDC)
Amlodipine Besylate 500 TABLET in 1 BOTTLE (68382-121-05)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-121-05
Package Description
500 TABLET in 1 BOTTLE (68382-121-05)
Product NDC
68382-121
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070921
Marketing Category Name
ANDA
Application Number
ANDA078226
Manufacturer
Zydus Pharmaceuticals USA 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/68382-121-05