"70518-4073-0" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE, PLASTIC (70518-4073-0)
(REMEDYREPACK INC.)

NDC Code70518-4073-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-4073-0)
Product NDC70518-4073
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20240509
Marketing Category NameANDA
Application NumberANDA078226
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength5
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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