Package 70518-3609-0
Brand: quetiapine fumarate
Generic: quetiapine fumaratePackage Facts
Identity
Package NDC
70518-3609-0
Digits Only
7051836090
Product NDC
70518-3609
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3609-0)
Marketing
Marketing Status
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": "414b97ad-12d2-7f31-e063-6294a90ab7a6", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312745"], "spl_set_id": ["da5c118f-404c-4453-aa10-a8656b1d7501"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3609-0)", "package_ndc": "70518-3609-0", "marketing_start_date": "20230104"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3609-1)", "package_ndc": "70518-3609-1", "marketing_start_date": "20251016"}], "brand_name": "Quetiapine Fumarate", "product_id": "70518-3609_414b97ad-12d2-7f31-e063-6294a90ab7a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-3609", "generic_name": "Quetiapine Fumarate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA091388", "marketing_category": "ANDA", "marketing_start_date": "20230104", "listing_expiration_date": "20261231"}