"72789-302-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-302-20
Package Description20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-302-20)
Product NDC72789-302
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070426
Marketing Category NameANDA
Application NumberANDA077859
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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