"69584-023-95" National Drug Code (NDC)

Amlodipine Besylate 5000 TABLET in 1 BOTTLE (69584-023-95)
(Oxford Pharmaceuticals, LLC)

NDC Code69584-023-95
Package Description5000 TABLET in 1 BOTTLE (69584-023-95)
Product NDC69584-023
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Proprietary Name Suffix10 Mg
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20211001
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerOxford Pharmaceuticals, LLC
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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