Package 68071-2459-1

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 68071-2459-1
Digits Only 6807124591
Product NDC 68071-2459
Product ID 68071-2459_2c6523b5-e13b-51f9-e063-6394a90a2f84
Description

100 TABLET in 1 BOTTLE (68071-2459-1)

Marketing

Marketing Status
Marketed Since 2021-06-24
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": "2c6523b5-e13b-51f9-e063-6394a90a2f84", "openfda": {"upc": ["0368071245912"], "unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["c577b306-ee7c-8364-e053-2a95a90abb13"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-2459-1)", "package_ndc": "68071-2459-1", "marketing_start_date": "20210624"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68071-2459_2c6523b5-e13b-51f9-e063-6394a90a2f84", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2459", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20071018", "listing_expiration_date": "20261231"}