"52125-801-19" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (52125-801-19)
(REMEDYREPACK INC.)

NDC Code52125-801-19
Package Description90 TABLET in 1 BOTTLE (52125-801-19)
Product NDC52125-801
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20131231
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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