Package 70518-4451-0

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 70518-4451-0
Digits Only 7051844510
Product NDC 70518-4451
Product ID 70518-4451_3ccf2a84-2a35-4fc2-e063-6294a90a84f1
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4451-0)

Marketing

Marketing Status
Marketed Since 2025-08-20
Brand quetiapine
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Quetiapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ccf2a84-2a35-4fc2-e063-6294a90a84f1", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312745"], "spl_set_id": ["b7aa0fce-1406-4665-a791-e30aed7b24ff"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4451-0)", "package_ndc": "70518-4451-0", "marketing_start_date": "20250820"}], "brand_name": "Quetiapine", "product_id": "70518-4451_3ccf2a84-2a35-4fc2-e063-6294a90a84f1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4451", "generic_name": "Quetiapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20250820", "listing_expiration_date": "20261231"}