Package 0904-6287-61

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0904-6287-61
Digits Only 0904628761
Product NDC 0904-6287
Product ID 0904-6287_8f57a36a-6427-4da3-ad7d-59093754fb98
Description

100 BLISTER PACK in 1 CARTON (0904-6287-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-04-23
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Olanzapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8f57a36a-6427-4da3-ad7d-59093754fb98", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639", "312077"], "spl_set_id": ["709d79a1-2742-4629-af43-161be166833a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6287-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6287-61", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "0904-6287_8f57a36a-6427-4da3-ad7d-59093754fb98", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6287", "generic_name": "Olanzapine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA076133", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}