"49349-662-02" National Drug Code (NDC)

Ciprofloxacin 30 TABLET in 1 BLISTER PACK (49349-662-02)
(REMEDYREPACK INC.)

NDC Code49349-662-02
Package Description30 TABLET in 1 BLISTER PACK (49349-662-02)
Product NDC49349-662
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20110121
End Marketing Date20171204
Marketing Category NameANDA
Application NumberANDA076794
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

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