"69150-113-01" National Drug Code (NDC)

Amlodipine Besylate 100 TABLET in 1 BOTTLE (69150-113-01)
(BIOMES PHARMACEUTICALS LLC)

NDC Code69150-113-01
Package Description100 TABLET in 1 BOTTLE (69150-113-01)
Product NDC69150-113
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20110415
Marketing Category NameANDA
Application NumberANDA077516
ManufacturerBIOMES PHARMACEUTICALS LLC
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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