Package 70518-4051-0

Brand: quetiapine extended release

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 70518-4051-0
Digits Only 7051840510
Product NDC 70518-4051
Product ID 70518-4051_3fa1b7c9-0ddc-66f7-e063-6294a90a9b6b
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4051-0)

Marketing

Marketing Status
Marketed Since 2024-04-13
Brand quetiapine extended release
Generic quetiapine
Sample Package No

Linked Drug Pages (1)

Quetiapine Extended Release ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fa1b7c9-0ddc-66f7-e063-6294a90a9b6b", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["895670"], "spl_set_id": ["995731f7-aace-4140-b699-d6e8975c7c83"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4051-0)", "package_ndc": "70518-4051-0", "marketing_start_date": "20240413"}], "brand_name": "Quetiapine Extended Release", "product_id": "70518-4051_3fa1b7c9-0ddc-66f7-e063-6294a90a9b6b", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4051", "generic_name": "Quetiapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA209635", "marketing_category": "ANDA", "marketing_start_date": "20240413", "listing_expiration_date": "20261231"}