"52125-069-02" National Drug Code (NDC)

Ciprofloxacin 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)
(REMEDYREPACK INC.)

NDC Code52125-069-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)
Product NDC52125-069
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130314
Marketing Category NameANDA
Application NumberANDA076558
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

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