"70518-2632-2" National Drug Code (NDC)

Amlodipine Besylate 7 TABLET in 1 BLISTER PACK (70518-2632-2)
(REMEDYREPACK INC.)

NDC Code70518-2632-2
Package Description7 TABLET in 1 BLISTER PACK (70518-2632-2)
Product NDC70518-2632
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200317
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerREMEDYREPACK INC.
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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