Package 0527-3164-32
Brand: olanzapine
Generic: olanzapinePackage Facts
Identity
Package NDC
0527-3164-32
Digits Only
0527316432
Product NDC
0527-3164
Description
30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0527-3164-32)
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": "002da62b-aec3-8e2a-e063-6294a90a5efc", "openfda": {"nui": ["N0000175430"], "upc": ["0305273163323", "0305273164320", "0305273161329", "0305273162326"], "unii": ["N7U69T4SZR"], "rxcui": ["312076", "314155", "351107", "351108"], "spl_set_id": ["002dd00f-7946-ea4f-e063-6294a90a5916"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0527-3164-32)", "package_ndc": "0527-3164-32", "marketing_start_date": "20230701"}], "brand_name": "Olanzapine", "product_id": "0527-3164_002da62b-aec3-8e2a-e063-6294a90a5efc", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0527-3164", "generic_name": "Olanzapine", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA208146", "marketing_category": "ANDA", "marketing_start_date": "20230530", "listing_expiration_date": "20261231"}