Package 71610-702-15

Brand: quetiapine

Generic: quetiapine
NDC Package

Package Facts

Identity

Package NDC 71610-702-15
Digits Only 7161070215
Product NDC 71610-702
Description

15 TABLET, FILM COATED in 1 BOTTLE (71610-702-15)

Marketing

Marketing Status
Marketed Since 2023-04-18
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": "1b43ca4a-8d47-4085-b50f-b282980f39e3", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["317174"], "spl_set_id": ["fdece055-aeb5-43d6-b730-54dd74bde304"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71610-702-15)", "package_ndc": "71610-702-15", "marketing_start_date": "20230418"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-702-30)", "package_ndc": "71610-702-30", "marketing_start_date": "20230418"}], "brand_name": "Quetiapine", "product_id": "71610-702_1b43ca4a-8d47-4085-b50f-b282980f39e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71610-702", "generic_name": "Quetiapine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA077745", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}