Package 68788-6835-3

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-6835-3
Digits Only 6878868353
Product NDC 68788-6835
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-6835-3)

Marketing

Marketing Status
Marketed Since 2016-11-21
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": "1a6f3793-c507-4d36-85da-0c482e695c6b", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["677c90cd-6527-40cb-a564-571796513fcb"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-6835-1)", "package_ndc": "68788-6835-1", "marketing_start_date": "20161121"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-6835-2)", "package_ndc": "68788-6835-2", "marketing_start_date": "20161121"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-6835-3)", "package_ndc": "68788-6835-3", "marketing_start_date": "20161121"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-6835-6)", "package_ndc": "68788-6835-6", "marketing_start_date": "20161121"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-6835-8)", "package_ndc": "68788-6835-8", "marketing_start_date": "20161121"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-6835-9)", "package_ndc": "68788-6835-9", "marketing_start_date": "20161121"}], "brand_name": "Sertraline Hydrochloride", "product_id": "68788-6835_1a6f3793-c507-4d36-85da-0c482e695c6b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-6835", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Preferred 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": "20161121", "listing_expiration_date": "20261231"}