Package 55700-851-90

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 55700-851-90
Digits Only 5570085190
Product NDC 55700-851
Product ID 55700-851_4e97913b-40ba-4158-a875-65496725b4e9
Description

90 TABLET in 1 BOTTLE (55700-851-90)

Marketing

Marketing Status
Discontinued 2026-10-31
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": "4e97913b-40ba-4158-a875-65496725b4e9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["6fc110ba-87e7-404e-9e00-b680f354c7b0"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-851-90)", "package_ndc": "55700-851-90", "marketing_end_date": "20261031", "marketing_start_date": "20200820"}], "brand_name": "Citalopram Hydrobromide", "product_id": "55700-851_4e97913b-40ba-4158-a875-65496725b4e9", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55700-851", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20200320"}