"72189-111-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)
(DIRECT RX)

NDC Code72189-111-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)
Product NDC72189-111
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200612
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerDIRECT RX
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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