Package 0904-6802-61
Brand: quetiapine
Generic: quetiapinePackage Facts
Identity
Package NDC
0904-6802-61
Digits Only
0904680261
Product NDC
0904-6802
Description
100 BLISTER PACK in 1 CARTON (0904-6802-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
Brand
quetiapine
Generic
quetiapine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d4de1de-a8d2-4cd6-b9a6-d38e2d009df7", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["b02324b1-e7f0-4cbc-8778-5f7c4a5d194a"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6802-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6802-61", "marketing_start_date": "20170822"}], "brand_name": "Quetiapine", "product_id": "0904-6802_3d4de1de-a8d2-4cd6-b9a6-d38e2d009df7", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-6802", "generic_name": "Quetiapine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA204203", "marketing_category": "ANDA", "marketing_start_date": "20170822", "listing_expiration_date": "20261231"}