Package 80425-0012-1

Brand: duloxetine hcl dr

Generic: duloxetine hcl
NDC Package

Package Facts

Identity

Package NDC 80425-0012-1
Digits Only 8042500121
Product NDC 80425-0012
Product ID 80425-0012_2a984d4a-2346-2be3-e063-6294a90ad5d4
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-1)

Marketing

Marketing Status
Marketed Since 2020-09-25
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": "2a984d4a-2346-2be3-e063-6294a90ad5d4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["af6f8abd-19ec-69e4-e053-2a95a90ab69e"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-1)", "package_ndc": "80425-0012-1", "marketing_start_date": "20200925"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-2)", "package_ndc": "80425-0012-2", "marketing_start_date": "20200925"}], "brand_name": "Duloxetine HCL DR", "product_id": "80425-0012_2a984d4a-2346-2be3-e063-6294a90ad5d4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0012", "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": "ANDA203197", "marketing_category": "ANDA", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}