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"71335-0122-8" National Drug Code (NDC)

Mirtazapine 21 TABLET, FILM COATED in 1 BOTTLE (71335-0122-8)
(Bryant Ranch Prepack)

NDC Code71335-0122-8
Package Description21 TABLET, FILM COATED in 1 BOTTLE (71335-0122-8)
Product NDC71335-0122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMirtazapine
Non-Proprietary NameMirtazapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070822
Marketing Category NameANDA
Application NumberANDA077666
ManufacturerBryant Ranch Prepack
Substance NameMIRTAZAPINE
Strength15
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0122-8





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