Package 70518-1748-1

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1748-1
Digits Only 7051817481
Product NDC 70518-1748
Product ID 70518-1748_49650dfa-0a3f-a8d0-e063-6394a90ad3c3
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1748-1)

Marketing

Marketing Status
Marketed Since 2019-04-11
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": "49650dfa-0a3f-a8d0-e063-6394a90ad3c3", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["575da603-b038-421f-9894-6796d9ac33cc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1748-1)", "package_ndc": "70518-1748-1", "marketing_start_date": "20190411"}], "brand_name": "Sertraline Hydrochloride", "product_id": "70518-1748_49650dfa-0a3f-a8d0-e063-6394a90ad3c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1748", "generic_name": "Sertraline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20190108", "listing_expiration_date": "20271231"}