Package 51655-680-26

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 51655-680-26
Digits Only 5165568026
Product NDC 51655-680
Product ID 51655-680_4950c3d6-8a7b-8e8f-e063-6294a90a015c
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-26)

Marketing

Marketing Status
Marketed Since 2022-05-04
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4950c3d6-8a7b-8e8f-e063-6294a90a015c", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["d9ccb3fb-b607-9491-e053-2995a90a39c9"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-26)", "package_ndc": "51655-680-26", "marketing_start_date": "20220504"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-52)", "package_ndc": "51655-680-52", "marketing_start_date": "20220302"}], "brand_name": "Citalopram", "product_id": "51655-680_4950c3d6-8a7b-8e8f-e063-6294a90a015c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-680", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20271231"}