"80425-0492-1" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE (80425-0492-1)
(Advanced Rx of Tennessee, LLC)

NDC Code80425-0492-1
Package Description20 TABLET in 1 BOTTLE (80425-0492-1)
Product NDC80425-0492
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofolxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20250202
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerAdvanced Rx of Tennessee, LLC
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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