Package 16729-132-12

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 16729-132-12
Digits Only 1672913212
Product NDC 16729-132
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-132-12)

Marketing

Marketing Status
Marketed Since 2017-11-30
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": "438fdf1f-3027-fb5a-e063-6294a90ac8d4", "openfda": {"upc": ["0316729132107"], "unii": ["2S3PL1B6UJ"], "rxcui": ["853201"], "spl_set_id": ["72111c36-c625-434f-9f16-7f25e0ff75f3"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-132-12)", "package_ndc": "16729-132-12", "marketing_start_date": "20171130"}], "brand_name": "QUETIAPINE FUMARATE", "product_id": "16729-132_438fdf1f-3027-fb5a-e063-6294a90ac8d4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16729-132", "generic_name": "QUETIAPINE FUMARATE", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUETIAPINE FUMARATE", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA206252", "marketing_category": "ANDA", "marketing_start_date": "20171130", "listing_expiration_date": "20261231"}