Package 17856-0564-1

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 17856-0564-1
Digits Only 1785605641
Product NDC 17856-0564
Product ID 17856-0564_34f3a909-1a50-3667-e063-6294a90aa4aa
Description

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0564-1) / 10 mL in 1 CUP, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2024-06-05
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": "34f3a909-1a50-3667-e063-6294a90aa4aa", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["2640311d-8b88-4513-9c80-a08390b8142a"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0564-1)  / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-0564-1", "marketing_start_date": "20240605"}], "brand_name": "Citalopram Hydrobromide", "product_id": "17856-0564_34f3a909-1a50-3667-e063-6294a90aa4aa", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "17856-0564", "generic_name": "Citalopram Hydrobromide", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201450", "marketing_category": "ANDA", "marketing_start_date": "20190531", "listing_expiration_date": "20261231"}