Package 71335-0480-1

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 71335-0480-1
Digits Only 7133504801
Product NDC 71335-0480
Description

30 TABLET in 1 BOTTLE (71335-0480-1)

Marketing

Marketing Status
Marketed Since 2018-02-26
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": "fc40aa2f-2477-4703-8749-cd7b8e8d4323", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["15cb00da-4435-4930-90d0-faadf2739a5c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0480-1)", "package_ndc": "71335-0480-1", "marketing_start_date": "20180226"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0480-2)", "package_ndc": "71335-0480-2", "marketing_start_date": "20241030"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0480-3)", "package_ndc": "71335-0480-3", "marketing_start_date": "20180426"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0480-4)", "package_ndc": "71335-0480-4", "marketing_start_date": "20180222"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0480-5)", "package_ndc": "71335-0480-5", "marketing_start_date": "20191111"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0480-6)", "package_ndc": "71335-0480-6", "marketing_start_date": "20230810"}], "brand_name": "Citalopram Hydrobromide", "product_id": "71335-0480_fc40aa2f-2477-4703-8749-cd7b8e8d4323", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0480", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}