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"0024-5820-15" National Drug Code (NDC)

Oforta 3 BLISTER PACK in 1 BOTTLE (0024-5820-15) > 5 TABLET, FILM COATED in 1 BLISTER PACK (0024-5820-05)
(sanofi-aventis U.S. LLC)

NDC Code0024-5820-15
Package Description3 BLISTER PACK in 1 BOTTLE (0024-5820-15) > 5 TABLET, FILM COATED in 1 BLISTER PACK (0024-5820-05)
Product NDC0024-5820
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOforta
Non-Proprietary NameFludarabine Phosphate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20091231
Marketing Category NameNDA
Application NumberNDA022273
Manufacturersanofi-aventis U.S. LLC
Substance NameFLUDARABINE PHOSPHATE
Strength10
Strength Unitmg/1
Pharmacy ClassesNucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0024-5820-15





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