"61919-054-10" National Drug Code (NDC)

Ciprofloxacin 10 TABLET in 1 BOTTLE (61919-054-10)
(Direct Rx)

NDC Code61919-054-10
Package Description10 TABLET in 1 BOTTLE (61919-054-10)
Product NDC61919-054
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerDirect Rx
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

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