celexa

Generic: citalopram

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name celexa
Generic Name citalopram
Labeler allergan, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0456-4020
Product ID 0456-4020_0eee9751-8886-474c-a806-8003e90cb151
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020822
Listing Expiration 2026-12-31
Marketing Start 1998-07-17

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04564020
Hyphenated Format 0456-4020

Supplemental Identifiers

RxCUI
200371 213344 213345 283672 284591 309314
UPC
0304564010018 0304564020017 0304564040015
UNII
I1E9D14F36

Packaging Origin

Original Packager
true

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 celexa (source: ndc)
Generic Name citalopram (source: ndc)
Application Number NDA020822 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0456-4020-01)
source: ndc

Packages (1)

0456-4020-01 100 TABLET, FILM COATED in 1 BOTTLE (0456-4020-01)

Ingredients (1)

citalopram hydrobromide (20 mg/1)

Linked Drug Pages (1)

Celexa ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0eee9751-8886-474c-a806-8003e90cb151", "openfda": {"upc": ["0304564010018", "0304564020017", "0304564040015"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "213344", "213345", "283672", "284591", "309314"], "spl_set_id": ["4259d9b1-de34-43a4-85a8-41dd214e9177"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0456-4020-01)", "package_ndc": "0456-4020-01", "marketing_start_date": "19980717"}], "brand_name": "Celexa", "product_id": "0456-4020_0eee9751-8886-474c-a806-8003e90cb151", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0456-4020", "generic_name": "citalopram", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Celexa", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "NDA020822", "marketing_category": "NDA", "marketing_start_date": "19980717", "listing_expiration_date": "20261231"}