"16714-652-03" National Drug Code (NDC)

Ciprofloxacin 1000 TABLET, FILM COATED in 1 BOTTLE (16714-652-03)
(NorthStar Rx LLC)

NDC Code16714-652-03
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (16714-652-03)
Product NDC16714-652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070426
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerNorthStar Rx LLC
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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