Package 70518-1040-0

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 70518-1040-0
Digits Only 7051810400
Product NDC 70518-1040
Product ID 70518-1040_484a09bb-a7f8-c9ea-e063-6394a90a4281
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1040-0)

Marketing

Marketing Status
Marketed Since 2018-03-01
Brand sertraline
Generic sertraline
Sample Package No

Linked Drug Pages (1)

Sertraline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "484a09bb-a7f8-c9ea-e063-6394a90a4281", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["e1864a7e-44b9-4399-9554-0c18b46fbdd6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1040-0)", "package_ndc": "70518-1040-0", "marketing_start_date": "20180301"}], "brand_name": "Sertraline", "product_id": "70518-1040_484a09bb-a7f8-c9ea-e063-6394a90a4281", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1040", "generic_name": "Sertraline", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20180301", "listing_expiration_date": "20271231"}