Package 68071-3766-9

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 68071-3766-9
Digits Only 6807137669
Product NDC 68071-3766
Product ID 68071-3766_2b61d5b5-490b-5494-e063-6294a90a3fa1
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)

Marketing

Marketing Status
Marketed Since 2025-01-10
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": "2b61d5b5-490b-5494-e063-6294a90a3fa1", "openfda": {"upc": ["0368071376692"], "unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["2b61c261-d7f2-4f9d-e063-6294a90acc24"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)", "package_ndc": "68071-3766-9", "marketing_start_date": "20250110"}], "brand_name": "Duloxetine", "product_id": "68071-3766_2b61d5b5-490b-5494-e063-6294a90a3fa1", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3766", "generic_name": "Duloxetine", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}