"43063-869-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code43063-869-20
Package Description20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)
Product NDC43063-869
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerPD-Rx Pharmaceuticals, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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