citalopram

Generic: citalopram hydrobromide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name citalopram
Generic Name citalopram hydrobromide
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

citalopram hydrobromide 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6433
Product ID 50090-6433_816c89dd-169a-4bb2-9651-a04adbc7f269
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077031
Listing Expiration 2026-12-31
Marketing Start 2004-10-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906433
Hyphenated Format 50090-6433

Supplemental Identifiers

RxCUI
200371
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 hydrobromide (source: ndc)
Application Number ANDA077031 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6433-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-6433-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-6433-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6433-3)
source: ndc

Packages (4)

50090-6433-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6433-0) 50090-6433-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6433-1) 50090-6433-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-6433-2) 50090-6433-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-6433-3)

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": "816c89dd-169a-4bb2-9651-a04adbc7f269", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["fc766b76-18c1-42cd-b276-f720f5821c11"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6433-0)", "package_ndc": "50090-6433-0", "marketing_start_date": "20230411"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6433-1)", "package_ndc": "50090-6433-1", "marketing_start_date": "20230411"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6433-2)", "package_ndc": "50090-6433-2", "marketing_start_date": "20230411"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6433-3)", "package_ndc": "50090-6433-3", "marketing_start_date": "20230417"}], "brand_name": "Citalopram", "product_id": "50090-6433_816c89dd-169a-4bb2-9651-a04adbc7f269", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6433", "generic_name": "Citalopram Hydrobromide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}