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"52125-917-10" National Drug Code (NDC)
Olanzapine 6 TABLET, FILM COATED in 1 BLISTER PACK (52125-917-10)
(REMEDYREPACK INC.)
NDC Code
52125-917-10
Package Description
6 TABLET, FILM COATED in 1 BLISTER PACK (52125-917-10)
Product NDC
52125-917
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Olanzapine
Non-Proprietary Name
Olanzapine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20160423
End Marketing Date
20170301
Marketing Category Name
ANDA
Application Number
ANDA076255
Manufacturer
REMEDYREPACK INC.
Substance Name
OLANZAPINE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Atypical Antipsychotic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-917-10