"65862-103-99" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (65862-103-99)
(Aurobindo Pharma Limited)

NDC Code65862-103-99
Package Description1000 TABLET in 1 BOTTLE (65862-103-99)
Product NDC65862-103
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20070717
Marketing Category NameANDA
Application NumberANDA078021
ManufacturerAurobindo Pharma Limited
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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