Package 70518-2175-0

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 70518-2175-0
Digits Only 7051821750
Product NDC 70518-2175
Product ID 70518-2175_49dabae4-2161-a05a-e063-6394a90a73d9
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2175-0)

Marketing

Marketing Status
Marketed Since 2019-07-01
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": "49dabae4-2161-a05a-e063-6394a90a73d9", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["616487"], "spl_set_id": ["479c9555-5d1e-4e5c-bfde-f3812829edd8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2175-0)", "package_ndc": "70518-2175-0", "marketing_start_date": "20190701"}], "brand_name": "Quetiapine Fumarate", "product_id": "70518-2175_49dabae4-2161-a05a-e063-6394a90a73d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2175", "generic_name": "Quetiapine Fumarate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA202674", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20271231"}