escitalopram oxalate

Generic: escitalopram oxalate

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

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/21

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7200
Product ID 50090-7200_c54a04b2-8d7d-4a25-8f53-aa075eea042b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202210
Listing Expiration 2026-12-31
Marketing Start 2024-01-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907200
Hyphenated Format 50090-7200

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 oxalate (source: ndc)
Generic Name escitalopram oxalate (source: ndc)
Application Number ANDA202210 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/21
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7200-1)
source: ndc

Packages (2)

50090-7200-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0) 50090-7200-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7200-1)

Ingredients (1)

escitalopram oxalate (20 mg/21)

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c54a04b2-8d7d-4a25-8f53-aa075eea042b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["c980262b-31f0-46df-902d-e593e1557fef"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7200-0)", "package_ndc": "50090-7200-0", "marketing_start_date": "20240730"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7200-1)", "package_ndc": "50090-7200-1", "marketing_start_date": "20240730"}], "brand_name": "Escitalopram Oxalate", "product_id": "50090-7200_c54a04b2-8d7d-4a25-8f53-aa075eea042b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7200", "generic_name": "Escitalopram Oxalate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/21"}], "application_number": "ANDA202210", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}