Package 72162-1058-3

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 72162-1058-3
Digits Only 7216210583
Product NDC 72162-1058
Description

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1058-3)

Marketing

Marketing Status
Marketed Since 2024-08-01
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6a478b7d-f27e-4e8e-9afb-ff8c53e2f93a", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["4673ccdd-c86c-4ddc-b462-941897ecfd22"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1058-3)", "package_ndc": "72162-1058-3", "marketing_start_date": "20240801"}], "brand_name": "Duloxetine", "product_id": "72162-1058_6a478b7d-f27e-4e8e-9afb-ff8c53e2f93a", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72162-1058", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}