Package 42291-695-10

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 42291-695-10
Digits Only 4229169510
Product NDC 42291-695
Product ID 42291-695_4871de67-6df0-716d-e063-6394a90a2195
Description

1000 TABLET, FILM COATED in 1 BOTTLE (42291-695-10)

Marketing

Marketing Status
Discontinued 2026-06-30
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": "4871de67-6df0-716d-e063-6394a90a2195", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312743", "312744", "312745", "317174", "616483", "616487"], "spl_set_id": ["8a3fc038-aad1-6404-6ead-a4a55127cf43"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42291-695-10)", "package_ndc": "42291-695-10", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}], "brand_name": "Quetiapine", "product_id": "42291-695_4871de67-6df0-716d-e063-6394a90a2195", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "42291-695", "generic_name": "Quetiapine", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "25 mg/1"}], "application_number": "ANDA077745", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}