Package 82009-107-05

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 82009-107-05
Digits Only 8200910705
Product NDC 82009-107
Product ID 82009-107_f85b3b65-e283-4270-895c-c601b6e7c6a6
Description

500 TABLET, FILM COATED in 1 BOTTLE (82009-107-05)

Marketing

Marketing Status
Marketed Since 2023-08-01
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": "f85b3b65-e283-4270-895c-c601b6e7c6a6", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["e0822069-9672-4d4c-bc1a-8739b0dd045c"], "manufacturer_name": ["QUALLENT PHARMACEUTICALS HEALTH LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (82009-107-05)", "package_ndc": "82009-107-05", "marketing_start_date": "20230801"}], "brand_name": "Citalopram", "product_id": "82009-107_f85b3b65-e283-4270-895c-c601b6e7c6a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "82009-107", "generic_name": "Citalopram Hydrobromide", "labeler_name": "QUALLENT PHARMACEUTICALS HEALTH 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": "20230801", "listing_expiration_date": "20261231"}