escitalopram

Generic: escitalopram

Labeler: quality care products, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler quality care products, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
Quality Care Products, LLC

Identifiers & Regulatory

Product NDC 55700-847
Product ID 55700-847_ce07bcac-80a7-47bf-a93d-8ef0c0a717ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078032
Marketing Start 2020-03-06
Marketing End 2026-07-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700847
Hyphenated Format 55700-847

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

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (55700-847-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (55700-847-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (55700-847-90)
source: ndc

Packages (3)

55700-847-30 30 TABLET, FILM COATED in 1 BOTTLE (55700-847-30) 55700-847-60 60 TABLET, FILM COATED in 1 BOTTLE (55700-847-60) 55700-847-90 90 TABLET, FILM COATED in 1 BOTTLE (55700-847-90)

Ingredients (1)

escitalopram oxalate (10 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": "ce07bcac-80a7-47bf-a93d-8ef0c0a717ee", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["dffdb225-c87c-4182-87be-b6a20ae14c85"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55700-847-30)", "package_ndc": "55700-847-30", "marketing_end_date": "20260727", "marketing_start_date": "20200306"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (55700-847-60)", "package_ndc": "55700-847-60", "marketing_end_date": "20260408", "marketing_start_date": "20200306"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55700-847-90)", "package_ndc": "55700-847-90", "marketing_end_date": "20260727", "marketing_start_date": "20200819"}], "brand_name": "Escitalopram", "product_id": "55700-847_ce07bcac-80a7-47bf-a93d-8ef0c0a717ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55700-847", "generic_name": "Escitalopram", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_end_date": "20260727", "marketing_start_date": "20200306"}