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 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5175
Product ID 50090-5175_af397ebb-a113-42d3-90d4-e8600b25809b
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 500905175
Hyphenated Format 50090-5175

Supplemental Identifiers

RxCUI
309314
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
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-5175-0)
  • 100 TABLET in 1 BOTTLE (50090-5175-1)
  • 90 TABLET in 1 BOTTLE (50090-5175-2)
source: ndc

Packages (3)

50090-5175-0 30 TABLET in 1 BOTTLE (50090-5175-0) 50090-5175-1 100 TABLET in 1 BOTTLE (50090-5175-1) 50090-5175-2 90 TABLET in 1 BOTTLE (50090-5175-2)

Ingredients (1)

citalopram hydrobromide (40 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": "af397ebb-a113-42d3-90d4-e8600b25809b", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["17af7a8d-ef57-4253-96ed-e457e0062eb5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5175-0)", "package_ndc": "50090-5175-0", "marketing_start_date": "20200925"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-5175-1)", "package_ndc": "50090-5175-1", "marketing_start_date": "20200925"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5175-2)", "package_ndc": "50090-5175-2", "marketing_start_date": "20200925"}], "brand_name": "Citalopram", "product_id": "50090-5175_af397ebb-a113-42d3-90d4-e8600b25809b", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-5175", "generic_name": "Citalopram", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}