Package 0228-2890-06

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 0228-2890-06
Digits Only 0228289006
Product NDC 0228-2890
Description

60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2890-06)

Marketing

Marketing Status
Marketed Since 2013-12-17
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": "15b6b091-1064-440e-8ab4-6b4eb28adcf4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["9dab9154-b86f-40dc-a4d1-18e6534dbc78"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2890-06)", "package_ndc": "0228-2890-06", "marketing_start_date": "20131217"}], "brand_name": "Duloxetine", "product_id": "0228-2890_15b6b091-1064-440e-8ab4-6b4eb28adcf4", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0228-2890", "generic_name": "Duloxetine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}