Package 61269-632-30

Brand: zyprexa

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 61269-632-30
Digits Only 6126963230
Product NDC 61269-632
Product ID 61269-632_40d4ed67-c51d-40d0-8a32-ecfdbf069f9a
Description

30 TABLET in 1 BOTTLE (61269-632-30)

Marketing

Marketing Status
Marketed Since 1996-10-01
Brand zyprexa
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Zyprexa, ZYPREXA Intramuscular, ZYPREXA Zydis ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40d4ed67-c51d-40d0-8a32-ecfdbf069f9a", "openfda": {"nui": ["N0000175430"], "upc": ["0361269633300", "0361269635304", "0361269634307", "0361269630309", "0361269632303", "0361269631306"], "unii": ["N7U69T4SZR"], "rxcui": ["153046", "153047", "153048", "200034", "212405", "261337", "283639", "284514", "312076", "312077", "312078", "312079", "314154", "314155", "351107", "351108", "485968", "545353", "754503", "754504", "754505", "754506"], "spl_set_id": ["b418946a-1ab4-4d89-a012-d94fc361a3c4"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["H2-Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (61269-632-30)", "package_ndc": "61269-632-30", "marketing_start_date": "19961001"}], "brand_name": "Zyprexa", "product_id": "61269-632_40d4ed67-c51d-40d0-8a32-ecfdbf069f9a", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "61269-632", "generic_name": "Olanzapine", "labeler_name": "H2-Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zyprexa", "active_ingredients": [{"name": "OLANZAPINE", "strength": "7.5 mg/1"}], "application_number": "NDA020592", "marketing_category": "NDA", "marketing_start_date": "19961001", "listing_expiration_date": "20271231"}