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"21695-210-10" National Drug Code (NDC)

Ciprofloxacin 10 TABLET, FILM COATED in 1 BOTTLE (21695-210-10)
(Rebel Distributors Corp.)

NDC Code21695-210-10
Package Description10 TABLET, FILM COATED in 1 BOTTLE (21695-210-10)
Product NDC21695-210
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20040609
Marketing Category NameANDA
Application NumberANDA076794
ManufacturerRebel Distributors Corp.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21695-210-10





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