"72789-519-10" National Drug Code (NDC)

Ciprofloxacin 10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-519-10
Package Description10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)
Product NDC72789-519
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofolxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20231001
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerPD-Rx Pharmaceuticals, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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