escitalopram

Generic: escitalopram

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7510
Product ID 68788-7510_5fbc446c-92d8-44ac-b4cc-dfba24c52881
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078032
Listing Expiration 2026-12-31
Marketing Start 2012-03-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887510
Hyphenated Format 68788-7510

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
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6)
  • 28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9)
source: ndc

Packages (5)

68788-7510-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1) 68788-7510-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3) 68788-7510-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6) 68788-7510-8 28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8) 68788-7510-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9)

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": "5fbc446c-92d8-44ac-b4cc-dfba24c52881", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["9889f7c0-fe0f-4267-a254-caee9f2b5eb0"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1)", "package_ndc": "68788-7510-1", "marketing_start_date": "20191227"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3)", "package_ndc": "68788-7510-3", "marketing_start_date": "20191227"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6)", "package_ndc": "68788-7510-6", "marketing_start_date": "20191227"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8)", "package_ndc": "68788-7510-8", "marketing_start_date": "20191227"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9)", "package_ndc": "68788-7510-9", "marketing_start_date": "20191227"}], "brand_name": "Escitalopram", "product_id": "68788-7510_5fbc446c-92d8-44ac-b4cc-dfba24c52881", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-7510", "generic_name": "Escitalopram", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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_start_date": "20120315", "listing_expiration_date": "20261231"}