"71335-1887-1" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE (71335-1887-1)
(Bryant Ranch Prepack)

NDC Code71335-1887-1
Package Description30 TABLET in 1 BOTTLE (71335-1887-1)
Product NDC71335-1887
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20110415
Marketing Category NameANDA
Application NumberANDA077516
ManufacturerBryant Ranch Prepack
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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