Package 82009-097-10

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 82009-097-10
Digits Only 8200909710
Product NDC 82009-097
Description

1000 TABLET in 1 BOTTLE (82009-097-10)

Marketing

Marketing Status
Marketed Since 2023-07-14
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c967a20e-cf1b-4bda-a63f-22ccdccef6aa", "openfda": {"upc": ["0382009097107", "0382009096100"], "unii": ["2S3PL1B6UJ"], "rxcui": ["312743", "312744", "317174", "616487"], "spl_set_id": ["d51c5bf6-950d-493b-be55-de575c5ef2e7"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-097-10)", "package_ndc": "82009-097-10", "marketing_start_date": "20230714"}], "brand_name": "Quetiapine fumarate", "product_id": "82009-097_c967a20e-cf1b-4bda-a63f-22ccdccef6aa", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82009-097", "generic_name": "quetiapine fumarate", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "100 mg/1"}], "application_number": "ANDA201109", "marketing_category": "ANDA", "marketing_start_date": "20230714", "listing_expiration_date": "20261231"}