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"72189-623-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE (72189-623-20)
(Direct_Rx)

NDC Code72189-623-20
Package Description20 TABLET in 1 BOTTLE (72189-623-20)
Product NDC72189-623
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20250514
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerDirect_Rx
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72189-623-20





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