Package 0378-6231-01

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 0378-6231-01
Digits Only 0378623101
Product NDC 0378-6231
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6231-01)

Marketing

Marketing Status
Marketed Since 2008-07-28
Brand citalopram
Generic citalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "55e0b75b-3772-4f5b-a162-1f70719daf3d", "openfda": {"upc": ["0303786232017", "0303786231010", "0303786233014"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["825c0c49-5fbf-6d8b-cb8c-94ebf0eda043"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6231-01)", "package_ndc": "0378-6231-01", "marketing_start_date": "20080728"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6231-05)", "package_ndc": "0378-6231-05", "marketing_start_date": "20080728"}], "brand_name": "Citalopram", "product_id": "0378-6231_55e0b75b-3772-4f5b-a162-1f70719daf3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0378-6231", "generic_name": "citalopram", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20080728", "listing_expiration_date": "20261231"}