Package 63187-429-30

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 63187-429-30
Digits Only 6318742930
Product NDC 63187-429
Product ID 63187-429_46cd719f-a6bc-4b3b-8ef5-860896fb787d
Description

30 TABLET, FILM COATED in 1 BOTTLE (63187-429-30)

Marketing

Marketing Status
Marketed Since 2015-02-02
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": "46cd719f-a6bc-4b3b-8ef5-860896fb787d", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "314154"], "spl_set_id": ["e40d54bf-7334-4418-8a87-ff85941adec1"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-429-30)", "package_ndc": "63187-429-30", "marketing_start_date": "20150202"}], "brand_name": "Olanzapine", "product_id": "63187-429_46cd719f-a6bc-4b3b-8ef5-860896fb787d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63187-429", "generic_name": "Olanzapine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}