Package 71610-957-74

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71610-957-74
Digits Only 7161095774
Product NDC 71610-957
Product ID 71610-957_41c54fc6-af9e-4506-e063-6294a90aedf0
Description

500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-957-74)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "41c54fc6-af9e-4506-e063-6294a90aedf0", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["41c54fb7-03f8-2326-e063-6394a90a6352"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-957-74)", "package_ndc": "71610-957-74", "marketing_start_date": "20251022"}], "brand_name": "Duloxetine", "product_id": "71610-957_41c54fc6-af9e-4506-e063-6294a90aedf0", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-957", "generic_name": "Duloxetine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}