Package 60760-559-30

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 60760-559-30
Digits Only 6076055930
Product NDC 60760-559
Product ID 60760-559_fbe5be69-0732-4e89-e053-6294a90a6fe8
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-559-30)

Marketing

Marketing Status
Marketed Since 2023-05-16
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

DULOXETINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fbe5be69-0732-4e89-e053-6294a90a6fe8", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["fbe58138-8e26-c4d9-e053-6294a90a3bd0"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-559-30)", "package_ndc": "60760-559-30", "marketing_start_date": "20230516"}], "brand_name": "DULOXETINE", "product_id": "60760-559_fbe5be69-0732-4e89-e053-6294a90a6fe8", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-559", "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": "ANDA206653", "marketing_category": "ANDA", "marketing_start_date": "20230516", "listing_expiration_date": "20261231"}