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"49349-194-02" National Drug Code (NDC)

Ciprofloxacin Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-194-02)
(REMEDYREPACK INC.)

NDC Code49349-194-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-194-02)
Product NDC49349-194
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin Hydrochloride
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110420
Marketing Category NameANDA
Application NumberANDA076794
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-194-02





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