Package 29300-312-16

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 29300-312-16
Digits Only 2930031216
Product NDC 29300-312
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-312-16)

Marketing

Marketing Status
Marketed Since 2022-09-12
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": "c5ece454-9c87-42df-a9f9-fc9806d7c312", "openfda": {"upc": ["0329300311167", "0329300312164", "0329300310160", "0329300309164"], "unii": ["2S3PL1B6UJ"], "rxcui": ["721791", "721794", "721796", "853201", "895670"], "spl_set_id": ["61695b42-cf71-43e3-8b5d-788fd439489f"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (29300-312-16)", "package_ndc": "29300-312-16", "marketing_start_date": "20220912"}], "brand_name": "Quetiapine", "product_id": "29300-312_c5ece454-9c87-42df-a9f9-fc9806d7c312", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "29300-312", "generic_name": "Quetiapine", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "400 mg/1"}], "application_number": "ANDA215478", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}