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"70518-1971-1" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE, PLASTIC (70518-1971-1)
(REMEDYREPACK INC.)

NDC Code70518-1971-1
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-1971-1)
Product NDC70518-1971
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20190320
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1971-1





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