Package 70518-2337-1

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-2337-1
Digits Only 7051823371
Product NDC 70518-2337
Product ID 70518-2337_4a034c6c-ff07-6450-e063-6294a90a843a
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2337-1)

Marketing

Marketing Status
Marketed Since 2025-08-06
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": "4a034c6c-ff07-6450-e063-6294a90a843a", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639"], "spl_set_id": ["9eb6b0d1-b301-4847-88f5-f8613d550ecc"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2337-1)", "package_ndc": "70518-2337-1", "marketing_start_date": "20250806"}], "brand_name": "Olanzapine", "product_id": "70518-2337_4a034c6c-ff07-6450-e063-6294a90a843a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2337", "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": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20191002", "listing_expiration_date": "20271231"}