Package 67046-1623-3

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 67046-1623-3
Digits Only 6704616233
Product NDC 67046-1623
Product ID 67046-1623_4615218b-35a5-a0f9-e063-6394a90a7c10
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1623-3)

Marketing

Marketing Status
Marketed Since 2025-12-16
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": "4615218b-35a5-a0f9-e063-6394a90a7c10", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791"], "spl_set_id": ["461523b5-8d12-9d96-e063-6394a90ad4c2"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1623-3)", "package_ndc": "67046-1623-3", "marketing_start_date": "20251216"}], "brand_name": "Quetiapine", "product_id": "67046-1623_4615218b-35a5-a0f9-e063-6394a90a7c10", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1623", "generic_name": "Quetiapine", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA215478", "marketing_category": "ANDA", "marketing_start_date": "20251216", "listing_expiration_date": "20261231"}