citalopram

Generic: citalopram

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

Drug Facts

Product Profile

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

citalopram hydrobromide 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5172
Product ID 50090-5172_3edc302b-9e97-403f-95fd-6c48d227de39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077534
Listing Expiration 2026-12-31
Marketing Start 2016-07-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905172
Hyphenated Format 50090-5172

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 (source: ndc)
Application Number ANDA077534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5172-0)
  • 60 TABLET in 1 BOTTLE (50090-5172-1)
  • 100 TABLET in 1 BOTTLE (50090-5172-2)
  • 90 TABLET in 1 BOTTLE (50090-5172-3)
source: ndc

Packages (4)

50090-5172-0 30 TABLET in 1 BOTTLE (50090-5172-0) 50090-5172-1 60 TABLET in 1 BOTTLE (50090-5172-1) 50090-5172-2 100 TABLET in 1 BOTTLE (50090-5172-2) 50090-5172-3 90 TABLET in 1 BOTTLE (50090-5172-3)

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": "3edc302b-9e97-403f-95fd-6c48d227de39", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["c91684c7-fddb-4cf0-9711-b0484c8c7e8b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5172-0)", "package_ndc": "50090-5172-0", "marketing_start_date": "20200925"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5172-1)", "package_ndc": "50090-5172-1", "marketing_start_date": "20200925"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-5172-2)", "package_ndc": "50090-5172-2", "marketing_start_date": "20200925"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5172-3)", "package_ndc": "50090-5172-3", "marketing_start_date": "20200925"}], "brand_name": "Citalopram", "product_id": "50090-5172_3edc302b-9e97-403f-95fd-6c48d227de39", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-5172", "generic_name": "Citalopram", "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": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}