Package 72789-088-60

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-088-60
Digits Only 7278908860
Product NDC 72789-088
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-088-60)

Marketing

Marketing Status
Marketed Since 2020-06-17
Brand sertraline hydrochloride
Generic sertraline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4031c5d9-ec99-51f3-e063-6294a90a4bcb", "openfda": {"upc": ["0372789088600"], "unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["91b4c802-9c6b-49bb-b5a7-661e1917ef34"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-088-60)", "package_ndc": "72789-088-60", "marketing_start_date": "20200617"}], "brand_name": "Sertraline Hydrochloride", "product_id": "72789-088_4031c5d9-ec99-51f3-e063-6294a90a4bcb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-088", "generic_name": "Sertraline Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}