Package 60760-462-60

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 60760-462-60
Digits Only 6076046260
Product NDC 60760-462
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-462-60)

Marketing

Marketing Status
Marketed Since 2025-09-16
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": "3ef10b7a-75bb-f47e-e063-6294a90ae315", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["9221f3e5-17b8-ea74-e053-2a95a90ad1a8"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-462-60)", "package_ndc": "60760-462-60", "marketing_start_date": "20250916"}], "brand_name": "Duloxetine", "product_id": "60760-462_3ef10b7a-75bb-f47e-e063-6294a90ae315", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-462", "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": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20190905", "listing_expiration_date": "20261231"}