Package 82009-032-10

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-032-10
Digits Only 8200903210
Product NDC 82009-032
Product ID 82009-032_c7833be1-34d9-43e4-8aff-966c14aa2798
Description

1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-032-10)

Marketing

Marketing Status
Marketed Since 2022-12-15
Brand duloxetine
Generic duloxetine hydrochloride
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": "c7833be1-34d9-43e4-8aff-966c14aa2798", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["31362045-201f-45f3-99f2-a5e322a0c30b"], "manufacturer_name": ["Quallent Pharmaceuticals Health, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-032-10)", "package_ndc": "82009-032-10", "marketing_start_date": "20221215"}], "brand_name": "Duloxetine", "product_id": "82009-032_c7833be1-34d9-43e4-8aff-966c14aa2798", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82009-032", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Quallent Pharmaceuticals Health, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}