Package 60760-495-30

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 60760-495-30
Digits Only 6076049530
Product NDC 60760-495
Product ID 60760-495_364689f2-275d-3160-e063-6394a90a0ce0
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)

Marketing

Marketing Status
Marketed Since 2025-05-29
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": "364689f2-275d-3160-e063-6394a90a0ce0", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["db900453-4777-4142-a236-5d3a6152d0a5"], "manufacturer_name": ["St Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-495-30)", "package_ndc": "60760-495-30", "marketing_start_date": "20250529"}], "brand_name": "Citalopram Hydrobromide", "product_id": "60760-495_364689f2-275d-3160-e063-6394a90a0ce0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-495", "generic_name": "Citalopram Hydrobromide", "labeler_name": "St Marys Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20140123", "listing_expiration_date": "20261231"}