Package 51655-043-52

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 51655-043-52
Digits Only 5165504352
Product NDC 51655-043
Product ID 51655-043_46ddbacb-b899-1715-e063-6394a90a3c49
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-52)

Marketing

Marketing Status
Marketed Since 2021-03-24
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": "46ddbacb-b899-1715-e063-6394a90a3c49", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["c133fc77-6c8a-d2b1-e053-2995a90ab5f7"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-26)", "package_ndc": "51655-043-26", "marketing_start_date": "20250422"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-52)", "package_ndc": "51655-043-52", "marketing_start_date": "20210324"}], "brand_name": "Citalopram Hydrobromide", "product_id": "51655-043_46ddbacb-b899-1715-e063-6394a90a3c49", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-043", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20210324", "listing_expiration_date": "20271231"}