"61786-819-19" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (61786-819-19)
(REMEDYREPACK INC.)

NDC Code61786-819-19
Package Description90 TABLET in 1 BOTTLE (61786-819-19)
Product NDC61786-819
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20160815
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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