Package 50090-6947-0

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 50090-6947-0
Digits Only 5009069470
Product NDC 50090-6947
Product ID 50090-6947_d88b94eb-00d5-4a10-988a-801d53865116
Description

90 TABLET in 1 BOTTLE (50090-6947-0)

Marketing

Marketing Status
Marketed Since 2023-12-18
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d88b94eb-00d5-4a10-988a-801d53865116", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["9059c8f1-8755-492d-aba2-5f5088ce69d3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6947-0)", "package_ndc": "50090-6947-0", "marketing_start_date": "20231218"}], "brand_name": "Citalopram Hydrobromide", "product_id": "50090-6947_d88b94eb-00d5-4a10-988a-801d53865116", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6947", "generic_name": "Citalopram Hydrobromide", "labeler_name": "A-S Medication Solutions", "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"}