Package 50090-7039-0

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 50090-7039-0
Digits Only 5009070390
Product NDC 50090-7039
Product ID 50090-7039_c28df410-62de-435b-b371-46b9130a831e
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7039-0)

Marketing

Marketing Status
Marketed Since 2024-01-11
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c28df410-62de-435b-b371-46b9130a831e", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["b244d4eb-8311-4663-8bca-dc08e88e5f5d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7039-0)", "package_ndc": "50090-7039-0", "marketing_start_date": "20240111"}], "brand_name": "Citalopram", "product_id": "50090-7039_c28df410-62de-435b-b371-46b9130a831e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7039", "generic_name": "Citalopram Hydrobromide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}