citalopram

Generic: citalopram

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-3329
Product ID 55154-3329_dd2b9818-2d9d-4109-bd46-30e45949d844
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078216
Listing Expiration 2027-12-31
Marketing Start 2009-11-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551543329
Hyphenated Format 55154-3329

Supplemental Identifiers

RxCUI
200371 283672
UPC
0055154332903 0055154334907
UNII
I1E9D14F36

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 ANDA078216 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-3329-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

55154-3329-0 10 BLISTER PACK in 1 BAG (55154-3329-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

citalopram hydrobromide (20 mg/1)

Linked Drug Pages (1)

Citalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dd2b9818-2d9d-4109-bd46-30e45949d844", "openfda": {"upc": ["0055154332903", "0055154334907"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["6c8942f8-963a-4007-a147-b77ac629e4d4"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3329-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-3329-0", "marketing_start_date": "20091102"}], "brand_name": "Citalopram", "product_id": "55154-3329_dd2b9818-2d9d-4109-bd46-30e45949d844", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-3329", "generic_name": "Citalopram", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20091102", "listing_expiration_date": "20271231"}