Package 51655-209-26
Brand: citalopram
Generic: citalopramPackage Facts
Identity
Package NDC
51655-209-26
Digits Only
5165520926
Product NDC
51655-209
Description
90 TABLET in 1 BOTTLE, PLASTIC (51655-209-26)
Marketing
Marketing Status
Brand
citalopram
Generic
citalopram
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2a0a2-f269-ef1d-e063-6394a90a49c2", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["f2b54f10-221f-5eed-e053-2995a90ab47f"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-209-26)", "package_ndc": "51655-209-26", "marketing_start_date": "20221021"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-209-52)", "package_ndc": "51655-209-52", "marketing_start_date": "20230103"}], "brand_name": "Citalopram", "product_id": "51655-209_48d2a0a2-f269-ef1d-e063-6394a90a49c2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-209", "generic_name": "Citalopram", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20221021", "listing_expiration_date": "20271231"}