Package 70518-1617-0

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 70518-1617-0
Digits Only 7051816170
Product NDC 70518-1617
Product ID 70518-1617_494f96d1-de22-da69-e063-6294a90aaa4f
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1617-0)

Marketing

Marketing Status
Marketed Since 2018-10-30
Brand sertraline
Generic sertraline
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "494f96d1-de22-da69-e063-6294a90aaa4f", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["c614be38-cb45-44a1-b78e-0cdfc0691618"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1617-0)", "package_ndc": "70518-1617-0", "marketing_start_date": "20181030"}], "brand_name": "Sertraline", "product_id": "70518-1617_494f96d1-de22-da69-e063-6294a90aaa4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1617", "generic_name": "Sertraline", "labeler_name": "REMEDYREPACK INC.", "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": "20181030", "listing_expiration_date": "20271231"}