Package 65862-657-03

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 65862-657-03
Digits Only 6586265703
Product NDC 65862-657
Product ID 65862-657_8449fc4c-9050-4a36-939b-bb3f93d16d7d
Description

3 BLISTER PACK in 1 CARTON (65862-657-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-657-10)

Marketing

Marketing Status
Marketed Since 2014-05-15
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": "8449fc4c-9050-4a36-939b-bb3f93d16d7d", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "spl_set_id": ["4d768cfe-3b20-4127-95b9-b4151b28afcc"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (65862-657-03)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-657-10)", "package_ndc": "65862-657-03", "marketing_start_date": "20140515"}], "brand_name": "Olanzapine", "product_id": "65862-657_8449fc4c-9050-4a36-939b-bb3f93d16d7d", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65862-657", "generic_name": "Olanzapine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA203708", "marketing_category": "ANDA", "marketing_start_date": "20140515", "listing_expiration_date": "20271231"}