Package 51655-137-26

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 51655-137-26
Digits Only 5165513726
Product NDC 51655-137
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-137-26)

Marketing

Marketing Status
Marketed Since 2023-01-19
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": "48c3e3f2-09c2-c403-e063-6294a90aafde", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["f2b42bdc-47e0-19c5-e053-2a95a90a1828"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-137-26)", "package_ndc": "51655-137-26", "marketing_start_date": "20230119"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-137-52)", "package_ndc": "51655-137-52", "marketing_start_date": "20221004"}], "brand_name": "Citalopram", "product_id": "51655-137_48c3e3f2-09c2-c403-e063-6294a90aafde", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-137", "generic_name": "Citalopram", "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": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20221004", "listing_expiration_date": "20271231"}