Package 68788-6429-6

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-6429-6
Digits Only 6878864296
Product NDC 68788-6429
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-6429-6)

Marketing

Marketing Status
Marketed Since 2016-06-28
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": "c7ed2451-d63a-4d50-a044-27a13a7727ac", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["5921f77f-01a2-40b9-ad77-2258865c997d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-6429-1)", "package_ndc": "68788-6429-1", "marketing_start_date": "20160628"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-6429-2)", "package_ndc": "68788-6429-2", "marketing_start_date": "20160628"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-6429-3)", "package_ndc": "68788-6429-3", "marketing_start_date": "20160628"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-6429-6)", "package_ndc": "68788-6429-6", "marketing_start_date": "20160628"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-6429-8)", "package_ndc": "68788-6429-8", "marketing_start_date": "20160628"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-6429-9)", "package_ndc": "68788-6429-9", "marketing_start_date": "20160628"}], "brand_name": "Sertraline Hydrochloride", "product_id": "68788-6429_c7ed2451-d63a-4d50-a044-27a13a7727ac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-6429", "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": "50 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20160628", "listing_expiration_date": "20261231"}