escitalopram

Generic: escitalopram

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

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2960
Product ID 71335-2960_11428fb6-bdb0-48ae-8e46-e2816dd13408
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090939
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 713352960
Hyphenated Format 71335-2960

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 (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number ANDA090939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)
source: ndc

Packages (1)

71335-2960-1 1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)

Ingredients (1)

escitalopram oxalate (20 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": "11428fb6-bdb0-48ae-8e46-e2816dd13408", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["1d2f83c1-8ffe-48f3-a084-150289001743"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)", "package_ndc": "71335-2960-1", "marketing_start_date": "20251022"}], "brand_name": "escitalopram", "product_id": "71335-2960_11428fb6-bdb0-48ae-8e46-e2816dd13408", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2960", "generic_name": "escitalopram", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}