Package 80425-0014-2

Brand: duloxetine hcl dr

Generic: duloxetine hcl
NDC Package

Package Facts

Identity

Package NDC 80425-0014-2
Digits Only 8042500142
Product NDC 80425-0014
Product ID 80425-0014_2a985779-9478-6d0e-e063-6294a90aa2a7
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-2)

Marketing

Marketing Status
Marketed Since 2022-12-11
Brand duloxetine hcl dr
Generic duloxetine hcl
Sample Package No

Linked Drug Pages (1)

Duloxetine HCL DR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a985779-9478-6d0e-e063-6294a90aa2a7", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["afd59273-75cb-5f33-e053-2995a90ab25f"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-1)", "package_ndc": "80425-0014-1", "marketing_start_date": "20221211"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-2)", "package_ndc": "80425-0014-2", "marketing_start_date": "20221211"}], "brand_name": "Duloxetine HCL DR", "product_id": "80425-0014_2a985779-9478-6d0e-e063-6294a90aa2a7", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0014", "generic_name": "Duloxetine HCL", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine HCL", "brand_name_suffix": "DR", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_start_date": "20221211", "listing_expiration_date": "20261231"}