Package 57237-017-60

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57237-017-60
Digits Only 5723701760
Product NDC 57237-017
Product ID 57237-017_96d64764-43ee-44ed-9bf0-600ec4f88981
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-017-60)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand duloxetine
Generic duloxetine hydrochloride
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": "96d64764-43ee-44ed-9bf0-600ec4f88981", "openfda": {"upc": ["0357237018309", "0357237017609", "0357237019306"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["ea2dc1a6-22d5-4295-9d39-9bf015dc5a89"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-017-60)", "package_ndc": "57237-017-60", "marketing_end_date": "20260430", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "57237-017_96d64764-43ee-44ed-9bf0-600ec4f88981", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "57237-017", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20131211"}