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"49349-612-03" National Drug Code (NDC)

Ciprofloxacin Hydrochloride 20 TABLET, FILM COATED in 1 BLISTER PACK (49349-612-03)
(REMEDYREPACK INC.)

NDC Code49349-612-03
Package Description20 TABLET, FILM COATED in 1 BLISTER PACK (49349-612-03)
Product NDC49349-612
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin Hydrochloride
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110315
Marketing Category NameANDA
Application NumberANDA075593
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-612-03





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