"67877-225-84" National Drug Code (NDC)

Mycophenolate Mofetil 3 BLISTER PACK in 1 CARTON (67877-225-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-225-84
Package Description3 BLISTER PACK in 1 CARTON (67877-225-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC67877-225
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMycophenolate Mofetil
Non-Proprietary NameMycophenolate Mofetil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20111128
Marketing Category NameANDA
Application NumberANDA091249
ManufacturerAscend Laboratories, LLC
Substance NameMYCOPHENOLATE MOFETIL
Strength500
Strength Unitmg/1
Pharmacy ClassesAntimetabolite Immunosuppressant [EPC]

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