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 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7177
Product ID 50090-7177_bff6c207-0f4b-42da-8aa1-d8fdd0e55188
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078777
Listing Expiration 2026-12-31
Marketing Start 2023-06-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907177
Hyphenated Format 50090-7177

Supplemental Identifiers

RxCUI
351249
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 ANDA078777 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7177-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7177-1)
source: ndc

Packages (2)

50090-7177-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-7177-0) 50090-7177-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7177-1)

Ingredients (1)

escitalopram oxalate (5 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": "bff6c207-0f4b-42da-8aa1-d8fdd0e55188", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["3965ca55-a5ff-4ed0-940c-363d74683fab"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7177-0)", "package_ndc": "50090-7177-0", "marketing_start_date": "20240530"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7177-1)", "package_ndc": "50090-7177-1", "marketing_start_date": "20240530"}], "brand_name": "escitalopram", "product_id": "50090-7177_bff6c207-0f4b-42da-8aa1-d8fdd0e55188", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7177", "generic_name": "escitalopram", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}