Package 72189-615-30
Brand: duloxetine d/r
Generic: duloxetine d/rPackage Facts
Identity
Package NDC
72189-615-30
Digits Only
7218961530
Product NDC
72189-615
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-30)
Marketing
Marketing Status
Brand
duloxetine d/r
Generic
duloxetine d/r
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35ced01c-03fc-4779-e063-6394a90a9cd5", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["2e58add7-b85e-2772-e063-6294a90a580d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-30)", "package_ndc": "72189-615-30", "marketing_start_date": "20250217"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-60)", "package_ndc": "72189-615-60", "marketing_start_date": "20250217"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-90)", "package_ndc": "72189-615-90", "marketing_start_date": "20250217"}], "brand_name": "Duloxetine D/R", "product_id": "72189-615_35ced01c-03fc-4779-e063-6394a90a9cd5", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72189-615", "generic_name": "Duloxetine D/R", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine D/R", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20250217", "listing_expiration_date": "20261231"}