Package 31722-564-24

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 31722-564-24
Digits Only 3172256424
Product NDC 31722-564
Description

240 mL in 1 BOTTLE (31722-564-24)

Marketing

Marketing Status
Marketed Since 2015-12-21
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1285242d-4c02-8735-e063-6294a90aa6ad", "openfda": {"upc": ["0331722564243"], "unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["dc7b3f88-ee55-4e3e-9ed4-fc06aa7620cc"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (31722-564-24)", "package_ndc": "31722-564-24", "marketing_start_date": "20151221"}], "brand_name": "Citalopram Hydrobromide", "product_id": "31722-564_1285242d-4c02-8735-e063-6294a90aa6ad", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "31722-564", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201450", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}