Package 68788-9692-1

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 68788-9692-1
Digits Only 6878896921
Product NDC 68788-9692
Description

100 TABLET, FILM COATED in 1 BOTTLE (68788-9692-1)

Marketing

Marketing Status
Marketed Since 2013-03-26
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "543a6dbf-f42d-4bc1-ad77-9ceac5e6bfe9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["b52acd68-fed1-4680-9eaf-b72e7dcba6fb"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-9692-1)", "package_ndc": "68788-9692-1", "marketing_start_date": "20130326"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-9692-3)", "package_ndc": "68788-9692-3", "marketing_start_date": "20130326"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-9692-6)", "package_ndc": "68788-9692-6", "marketing_start_date": "20130326"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-9692-8)", "package_ndc": "68788-9692-8", "marketing_start_date": "20130326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-9692-9)", "package_ndc": "68788-9692-9", "marketing_start_date": "20130326"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68788-9692_543a6dbf-f42d-4bc1-ad77-9ceac5e6bfe9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-9692", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20130326", "listing_expiration_date": "20271231"}