Package 0904-6376-61
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
0904-6376-61
Digits Only
0904637661
Product NDC
0904-6376
Description
100 BLISTER PACK in 1 CARTON (0904-6376-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
olanzapine
Generic
olanzapine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "efc47d5e-306c-464d-92a4-5156031202cf", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078", "314154"], "spl_set_id": ["0ecbf540-572e-4ca4-b694-18ca1cd1c194"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6376-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6376-61", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "0904-6376_efc47d5e-306c-464d-92a4-5156031202cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6376", "generic_name": "Olanzapine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}