escitalopram

Generic: escitalopram

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

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6534
Product ID 50090-6534_488baa4a-7e4b-47f3-94b2-8aa729de9cce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078032
Listing Expiration 2026-12-31
Marketing Start 2016-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906534
Hyphenated Format 50090-6534

Supplemental Identifiers

RxCUI
351250
UNII
5U85DBW7LO

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 escitalopram (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number ANDA078032 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)
source: ndc

Packages (2)

50090-6534-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0) 50090-6534-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)

Ingredients (1)

escitalopram oxalate (20 mg/1)

Linked Drug Pages (1)

Escitalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "488baa4a-7e4b-47f3-94b2-8aa729de9cce", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["2ffc6ec3-830f-46bc-9b3f-7c42cefa39b2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6534-0)", "package_ndc": "50090-6534-0", "marketing_start_date": "20230628"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6534-1)", "package_ndc": "50090-6534-1", "marketing_start_date": "20230628"}], "brand_name": "Escitalopram", "product_id": "50090-6534_488baa4a-7e4b-47f3-94b2-8aa729de9cce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6534", "generic_name": "Escitalopram", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}