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"52343-067-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BOTTLE (52343-067-20)
(Gen-Source Rx)

NDC Code52343-067-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (52343-067-20)
Product NDC52343-067
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070426
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerGen-Source Rx
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52343-067-20





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