Package 0904-6641-61

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 0904-6641-61
Digits Only 0904664161
Product NDC 0904-6641
Product ID 0904-6641_50f28d31-26e7-46fb-8bcb-207554f50708
Description

100 BLISTER PACK in 1 CARTON (0904-6641-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2013-03-01
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": "50f28d31-26e7-46fb-8bcb-207554f50708", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312743", "312744", "312745", "317174", "616483", "616487"], "spl_set_id": ["f9447739-9e21-4232-950f-174c0496ab66"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6641-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6641-61", "marketing_start_date": "20130301"}], "brand_name": "Quetiapine", "product_id": "0904-6641_50f28d31-26e7-46fb-8bcb-207554f50708", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6641", "generic_name": "Quetiapine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20271231"}