Package 70518-2113-0

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 70518-2113-0
Digits Only 7051821130
Product NDC 70518-2113
Product ID 70518-2113_2f8a6c7b-1e01-eaaa-e063-6294a90a988d
Description

30 TABLET in 1 BLISTER PACK (70518-2113-0)

Marketing

Marketing Status
Marketed Since 2019-05-23
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (1)

Quetiapine Fumarate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f8a6c7b-1e01-eaaa-e063-6294a90a988d", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312745"], "spl_set_id": ["a98cbbbd-e8da-4d0b-b6b1-56de0e1ba338"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2113-0)", "package_ndc": "70518-2113-0", "marketing_start_date": "20190523"}], "brand_name": "Quetiapine Fumarate", "product_id": "70518-2113_2f8a6c7b-1e01-eaaa-e063-6294a90a988d", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2113", "generic_name": "Quetiapine Fumarate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20190523", "listing_expiration_date": "20261231"}