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"69150-113-10" National Drug Code (NDC)

Amlodipine Besylate 1000 TABLET in 1 BOTTLE (69150-113-10)
(BIOMES PHARMACEUTICALS LLC)

NDC Code69150-113-10
Package Description1000 TABLET in 1 BOTTLE (69150-113-10)
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 [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69150-113-10





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