Package 60760-461-30
Brand: duloxetine
Generic: duloxetinePackage Facts
Identity
Package NDC
60760-461-30
Digits Only
6076046130
Product NDC
60760-461
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-461-30)
Marketing
Marketing Status
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": "45745bf3-a131-b51a-e063-6394a90a712e", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["9221aea1-8de1-b94e-e053-2a95a90a1eae"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-461-30)", "package_ndc": "60760-461-30", "marketing_start_date": "20190905"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-461-60)", "package_ndc": "60760-461-60", "marketing_start_date": "20191021"}], "brand_name": "Duloxetine", "product_id": "60760-461_45745bf3-a131-b51a-e063-6394a90a712e", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-461", "generic_name": "Duloxetine", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20190905", "listing_expiration_date": "20261231"}