Package 67046-1483-3

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1483-3
Digits Only 6704614833
Product NDC 67046-1483
Product ID 67046-1483_2ce04fcc-4bad-22dc-e063-6294a90af8a9
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1483-3)

Marketing

Marketing Status
Marketed Since 2025-01-29
Brand sertraline hydrochloride
Generic sertraline hydrochloride
Sample Package No

Linked Drug Pages (1)

Sertraline hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ce04fcc-4bad-22dc-e063-6294a90af8a9", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["2ce05049-030f-3e8b-e063-6394a90a4885"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1483-3)", "package_ndc": "67046-1483-3", "marketing_start_date": "20250129"}], "brand_name": "Sertraline hydrochloride", "product_id": "67046-1483_2ce04fcc-4bad-22dc-e063-6294a90af8a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "67046-1483", "generic_name": "Sertraline hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA078403", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}