Package 0093-5247-65
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
0093-5247-65
Digits Only
0093524765
Product NDC
0093-5247
Description
30 BLISTER PACK in 1 CARTON (0093-5247-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5247-19)
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": "cca528be-51eb-41ca-881a-0e57d49cf94a", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312076", "314155", "351107", "351108"], "spl_set_id": ["dd0b2525-4e2f-44fc-9302-0ae4ebb1e135"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0093-5247-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5247-19)", "package_ndc": "0093-5247-65", "marketing_start_date": "20120224"}], "brand_name": "Olanzapine", "product_id": "0093-5247_cca528be-51eb-41ca-881a-0e57d49cf94a", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0093-5247", "generic_name": "Olanzapine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA077243", "marketing_category": "ANDA", "marketing_start_date": "20120124", "listing_expiration_date": "20271231"}