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"0002-7140-01" National Drug Code (NDC)

Reopro 5 mL in 1 VIAL, SINGLE-USE (0002-7140-01)
(Eli Lilly and Company)

NDC Code0002-7140-01
Package Description5 mL in 1 VIAL, SINGLE-USE (0002-7140-01)
Product NDC0002-7140
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameReopro
Non-Proprietary NameAbciximab
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS
Start Marketing Date19931216
End Marketing Date20190131
Marketing Category NameBLA
Application NumberBLA103575
ManufacturerEli Lilly and Company
Substance NameABCIXIMAB
Strength2
Strength Unitmg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0002-7140-01





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