"13107-076-30" National Drug Code (NDC)

Ciprofloxacin 30 TABLET, FILM COATED in 1 BOTTLE (13107-076-30)
(Aurolife Pharma LLC)

NDC Code13107-076-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (13107-076-30)
Product NDC13107-076
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090801
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerAurolife Pharma LLC
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

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