Package 82009-171-10

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 82009-171-10
Digits Only 8200917110
Product NDC 82009-171
Product ID 82009-171_8bd1cf58-1f36-4c7e-a549-24bb4ec3e154
Description

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-171-10)

Marketing

Marketing Status
Marketed Since 2025-07-01
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

Duloxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8bd1cf58-1f36-4c7e-a549-24bb4ec3e154", "openfda": {"upc": ["0382009172309", "0382009171104", "0382009173108", "0382009170107"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["b3b26383-9924-40f9-b4bb-43e30b70493e"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-171-10)", "package_ndc": "82009-171-10", "marketing_start_date": "20250701"}], "brand_name": "Duloxetine", "product_id": "82009-171_8bd1cf58-1f36-4c7e-a549-24bb4ec3e154", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82009-171", "generic_name": "Duloxetine", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}