Package 67046-1451-3

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 67046-1451-3
Digits Only 6704614513
Product NDC 67046-1451
Product ID 67046-1451_2d94184b-be29-ca5f-e063-6294a90afd1c
Description

30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1451-3)

Marketing

Marketing Status
Marketed Since 2025-02-07
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": "2d94184b-be29-ca5f-e063-6294a90afd1c", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["2d942e38-90d4-de39-e063-6294a90a9822"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1451-3)", "package_ndc": "67046-1451-3", "marketing_start_date": "20250207"}], "brand_name": "Duloxetine", "product_id": "67046-1451_2d94184b-be29-ca5f-e063-6294a90afd1c", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67046-1451", "generic_name": "Duloxetine", "labeler_name": "Coupler LLC", "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": "20250207", "listing_expiration_date": "20261231"}