"70518-0239-0" National Drug Code (NDC)

Quetiapine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0239-0)
(REMEDYREPACK INC.)

NDC Code70518-0239-0
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0239-0)
Product NDC70518-0239
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameQuetiapine
Non-Proprietary NameQuetiapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170220
Marketing Category NameANDA
Application NumberANDA202152
ManufacturerREMEDYREPACK INC.
Substance NameQUETIAPINE FUMARATE
Strength300
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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