Package 50268-769-15

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 50268-769-15
Digits Only 5026876915
Product NDC 50268-769
Description

50 BLISTER PACK in 1 BOX (50268-769-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-769-11)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand sertraline
Generic sertraline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48364c4d-880c-1d77-e063-6294a90a9011", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["10baaffd-061e-d665-e063-6294a90a1594"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-769-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-769-11)", "package_ndc": "50268-769-15", "marketing_start_date": "20240206"}], "brand_name": "Sertraline", "product_id": "50268-769_48364c4d-880c-1d77-e063-6294a90a9011", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50268-769", "generic_name": "Sertraline", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20240206", "listing_expiration_date": "20271231"}