Package 68071-3775-9

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 68071-3775-9
Digits Only 6807137759
Product NDC 68071-3775
Product ID 68071-3775_2c28879c-0117-f2ff-e063-6394a90a5c30
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3775-9)

Marketing

Marketing Status
Marketed Since 2025-01-20
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": "2c28879c-0117-f2ff-e063-6394a90a5c30", "openfda": {"upc": ["0368071377590"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["2c288791-2d8f-84bb-e063-6294a90a7e1e"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3775-9)", "package_ndc": "68071-3775-9", "marketing_start_date": "20250120"}], "brand_name": "Duloxetine", "product_id": "68071-3775_2c28879c-0117-f2ff-e063-6394a90a5c30", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3775", "generic_name": "Duloxetine", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}