citalopram
Generic: citalopram
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
citalopram
Generic Name
citalopram
Labeler
golden state medical supply, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
citalopram hydrobromide 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60429-175
Product ID
60429-175_2bb26393-e61c-3ff0-e063-6394a90aea5e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077045
Listing Expiration
2026-12-31
Marketing Start
2005-04-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60429175
Hyphenated Format
60429-175
Supplemental Identifiers
RxCUI
UNII
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
ANDA077045 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 1000 TABLET, FILM COATED in 1 BOTTLE (60429-175-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bb26393-e61c-3ff0-e063-6394a90aea5e", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["f3a26d92-b662-4896-82eb-261948042408"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60429-175-10)", "package_ndc": "60429-175-10", "marketing_start_date": "20110520"}], "brand_name": "CITALOPRAM", "product_id": "60429-175_2bb26393-e61c-3ff0-e063-6394a90aea5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60429-175", "generic_name": "citalopram", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CITALOPRAM", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077045", "marketing_category": "ANDA", "marketing_start_date": "20050429", "listing_expiration_date": "20261231"}