Package 60429-175-10

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 60429-175-10
Digits Only 6042917510
Product NDC 60429-175
Description

1000 TABLET, FILM COATED in 1 BOTTLE (60429-175-10)

Marketing

Marketing Status
Marketed Since 2011-05-20
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": "2bb26393-e61c-3ff0-e063-6394a90aea5e", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["f3a26d92-b662-4896-82eb-261948042408"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60429-175-10)", "package_ndc": "60429-175-10", "marketing_start_date": "20110520"}], "brand_name": "CITALOPRAM", "product_id": "60429-175_2bb26393-e61c-3ff0-e063-6394a90aea5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60429-175", "generic_name": "citalopram", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CITALOPRAM", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077045", "marketing_category": "ANDA", "marketing_start_date": "20050429", "listing_expiration_date": "20261231"}