"70748-262-02" National Drug Code (NDC)

Mycophenolate Mofetil 500 TABLET in 1 BOTTLE (70748-262-02)
(Lupin Pharmaceuticals, Inc.)

NDC Code70748-262-02
Package Description500 TABLET in 1 BOTTLE (70748-262-02)
Product NDC70748-262
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMycophenolate Mofetil
Non-Proprietary NameMycophenolate Mofetil
Dosage FormTABLET
UsageORAL
Start Marketing Date20201221
End Marketing Date20240331
Marketing Category NameANDA
Application NumberANDA212087
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameMYCOPHENOLATE MOFETIL
Strength500
Strength Unitmg/1
Pharmacy ClassesAntimetabolite Immunosuppressant [EPC]

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