citalopram
Generic: citalopram
Labeler: chartwell governmental & specialty rx, llc.Drug Facts
Product Profile
Brand Name
citalopram
Generic Name
citalopram
Labeler
chartwell governmental & specialty rx, llc.
Dosage Form
SOLUTION
Routes
Active Ingredients
citalopram hydrobromide 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68999-540
Product ID
68999-540_484c3f19-d5f7-3e00-e063-6394a90a1938
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077629
Listing Expiration
2027-12-31
Marketing Start
2006-06-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68999540
Hyphenated Format
68999-540
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
citalopram (source: ndc)
Generic Name
citalopram (source: ndc)
Application Number
ANDA077629 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
Packaging
- 2 TRAY in 1 BOX (68999-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "484c3f19-d5f7-3e00-e063-6394a90a1938", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["3114274f-d81f-4b1f-8f17-35db9eee2ffe"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)", "package_ndc": "68999-540-24", "marketing_start_date": "20260113"}], "brand_name": "Citalopram", "product_id": "68999-540_484c3f19-d5f7-3e00-e063-6394a90a1938", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68999-540", "generic_name": "Citalopram", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077629", "marketing_category": "ANDA", "marketing_start_date": "20060614", "listing_expiration_date": "20271231"}