Package 70518-1582-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-1582-0
Digits Only 7051815820
Product NDC 70518-1582
Product ID 70518-1582_494dfc75-c2f2-1ebc-e063-6294a90ae1b0
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1582-0)

Marketing

Marketing Status
Marketed Since 2018-10-24
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": "494dfc75-c2f2-1ebc-e063-6294a90ae1b0", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639"], "spl_set_id": ["ad350abc-a1fc-4be4-b2be-c629121552a0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1582-0)", "package_ndc": "70518-1582-0", "marketing_start_date": "20181024"}], "brand_name": "Olanzapine", "product_id": "70518-1582_494dfc75-c2f2-1ebc-e063-6294a90ae1b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1582", "generic_name": "Olanzapine", "labeler_name": "REMEDYREPACK INC.", "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": "20181024", "listing_expiration_date": "20271231"}