"61786-735-02" National Drug Code (NDC)

Olanzapine 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-735-02)
(REMEDYREPACK INC.)

NDC Code61786-735-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (61786-735-02)
Product NDC61786-735
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlanzapine
Non-Proprietary NameOlanzapine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160607
Marketing Category NameANDA
Application NumberANDA076133
ManufacturerREMEDYREPACK INC.
Substance NameOLANZAPINE
Strength20
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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