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"70518-0316-0" National Drug Code (NDC)

Mirtazapine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0316-0)
(REMEDYREPACK INC.)

NDC Code70518-0316-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0316-0)
Product NDC70518-0316
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMirtazapine
Non-Proprietary NameMirtazapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170314
Marketing Category NameANDA
Application NumberANDA076921
ManufacturerREMEDYREPACK INC.
Substance NameMIRTAZAPINE
Strength30
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0316-0





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