"61919-361-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE (61919-361-20)
(DIRECT RX)

NDC Code61919-361-20
Package Description20 TABLET in 1 BOTTLE (61919-361-20)
Product NDC61919-361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20161116
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerDIRECT RX
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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