escitalopram

Generic: escitalopram oxalate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram oxalate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9687
Product ID 71335-9687_fada57d1-668f-4890-9873-f48716441db1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090432
Listing Expiration 2026-12-31
Marketing Start 2012-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359687
Hyphenated Format 71335-9687

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 oxalate (source: ndc)
Application Number ANDA090432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)
source: ndc

Packages (4)

71335-9687-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1) 71335-9687-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2) 71335-9687-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3) 71335-9687-4 100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)

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": "fada57d1-668f-4890-9873-f48716441db1", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["ee5963ad-3b53-48e5-b7a9-b13af5740ef1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-9687-1)", "package_ndc": "71335-9687-1", "marketing_start_date": "20230622"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-9687-2)", "package_ndc": "71335-9687-2", "marketing_start_date": "20230404"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-9687-3)", "package_ndc": "71335-9687-3", "marketing_start_date": "20230710"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-9687-4)", "package_ndc": "71335-9687-4", "marketing_start_date": "20241101"}], "brand_name": "Escitalopram", "product_id": "71335-9687_fada57d1-668f-4890-9873-f48716441db1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-9687", "generic_name": "Escitalopram Oxalate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}