escitalopram oxalate

Generic: escitalopram oxalate

Labeler: pharmasource meds, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram oxalate
Labeler pharmasource meds, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
Pharmasource Meds, LLC

Identifiers & Regulatory

Product NDC 82982-065
Product ID 82982-065_198ba216-39a7-3d98-e063-6394a90a9f0b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090939
Marketing Start 2023-05-01
Marketing End 2026-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82982065
Hyphenated Format 82982-065

Supplemental Identifiers

RxCUI
349332
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 ANDA090939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (82982-065-60)
source: ndc

Packages (1)

82982-065-60 60 TABLET in 1 BOTTLE (82982-065-60)

Ingredients (1)

escitalopram oxalate (10 mg/1)

Linked Drug Pages (1)

escitalopram oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "198ba216-39a7-3d98-e063-6394a90a9f0b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["faa48e9c-a34c-c745-e053-6294a90a9b21"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (82982-065-60)", "package_ndc": "82982-065-60", "marketing_end_date": "20260731", "marketing_start_date": "20230501"}], "brand_name": "escitalopram oxalate", "product_id": "82982-065_198ba216-39a7-3d98-e063-6394a90a9f0b", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "82982-065", "generic_name": "escitalopram oxalate", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20230501"}