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"61919-735-90" National Drug Code (NDC)

Ciprofloxacin 90 TABLET in 1 BOTTLE (61919-735-90)
(DIRECT RX)

NDC Code61919-735-90
Package Description90 TABLET in 1 BOTTLE (61919-735-90)
Product NDC61919-735
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160912
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerDIRECT RX
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength750
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-735-90





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