Package 68084-529-01

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 68084-529-01
Digits Only 6808452901
Product NDC 68084-529
Product ID 68084-529_186bfffc-1308-b7be-e063-6394a90a0d6b
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-529-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-529-11)

Marketing

Marketing Status
Marketed Since 2012-05-08
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": "186bfffc-1308-b7be-e063-6394a90a0d6b", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639", "312077"], "spl_set_id": ["c0d705bf-b719-4c7b-b83d-c17d41cbbfad"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-529-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-529-11)", "package_ndc": "68084-529-01", "marketing_start_date": "20120508"}], "brand_name": "Olanzapine", "product_id": "68084-529_186bfffc-1308-b7be-e063-6394a90a0d6b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68084-529", "generic_name": "Olanzapine", "labeler_name": "American Health Packaging", "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": "20120508", "listing_expiration_date": "20261231"}