Package 70518-1611-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-1611-0
Digits Only 7051816110
Product NDC 70518-1611
Product ID 70518-1611_494f4e23-fd6a-1e40-e063-6394a90ae99f
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-0)

Marketing

Marketing Status
Marketed Since 2018-10-29
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "494f4e23-fd6a-1e40-e063-6394a90ae99f", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312079"], "spl_set_id": ["68de2a51-69b2-4d99-be79-36a95a4bc475"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-0)", "package_ndc": "70518-1611-0", "marketing_start_date": "20181029"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-2)", "package_ndc": "70518-1611-2", "marketing_start_date": "20250207"}], "brand_name": "Olanzapine", "product_id": "70518-1611_494f4e23-fd6a-1e40-e063-6394a90ae99f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1611", "generic_name": "Olanzapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20271231"}