Package 71610-412-60

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 71610-412-60
Digits Only 7161041260
Product NDC 71610-412
Description

90 TABLET in 1 BOTTLE (71610-412-60)

Marketing

Marketing Status
Marketed Since 2020-03-30
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": "7c318729-6d4b-4a2a-a2fe-155b6513e7d4", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["0867140e-a483-4bf7-8326-4a9730cc9d9d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-412-60)", "package_ndc": "71610-412-60", "marketing_start_date": "20200330"}], "brand_name": "Citalopram", "product_id": "71610-412_7c318729-6d4b-4a2a-a2fe-155b6513e7d4", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-412", "generic_name": "Citalopram", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}