"70518-1352-0" National Drug Code (NDC)

Mirtazapine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1352-0)
(REMEDYREPACK INC.)

NDC Code70518-1352-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1352-0)
Product NDC70518-1352
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMirtazapine
Non-Proprietary NameMirtazapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180807
Marketing Category NameANDA
Application NumberANDA077666
ManufacturerREMEDYREPACK INC.
Substance NameMIRTAZAPINE
Strength15
Strength Unitmg/1

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