citalopram
Generic: citalopram
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
citalopram
Generic Name
citalopram
Labeler
chartwell rx, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
citalopram hydrobromide 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
62135-540
Product ID
62135-540_4a2ccdf3-3193-9182-e063-6294a90ad893
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
62135540
Hyphenated Format
62135-540
Supplemental Identifiers
RxCUI
UPC
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 (62135-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (62135-540-10)
- 473 mL in 1 BOTTLE (62135-540-47)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a2ccdf3-3193-9182-e063-6294a90ad893", "openfda": {"upc": ["0362135540470"], "unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["b1f0c6e8-85eb-4368-8709-9cace32415cb"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (62135-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (62135-540-10)", "package_ndc": "62135-540-24", "marketing_start_date": "20250403"}, {"sample": false, "description": "473 mL in 1 BOTTLE (62135-540-47)", "package_ndc": "62135-540-47", "marketing_start_date": "20221031"}], "brand_name": "Citalopram", "product_id": "62135-540_4a2ccdf3-3193-9182-e063-6294a90ad893", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "62135-540", "generic_name": "Citalopram", "labeler_name": "Chartwell 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"}