Package 68071-3519-3

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 68071-3519-3
Digits Only 6807135193
Product NDC 68071-3519
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3519-3)

Marketing

Marketing Status
Marketed Since 2023-10-10
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": "2d04f6ef-7b85-88b9-e063-6294a90a87f8", "openfda": {"upc": ["0368071351934"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["075fc7c9-7b4b-b9c3-e063-6394a90a926e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3519-3)", "package_ndc": "68071-3519-3", "marketing_start_date": "20231010"}], "brand_name": "Duloxetine", "product_id": "68071-3519_2d04f6ef-7b85-88b9-e063-6294a90a87f8", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3519", "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": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}