escitalopram

Generic: escitalopram

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-325
Product ID 71205-325_65ffd6fd-533b-4e39-8fbc-5c65cd88d602
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202389
Listing Expiration 2026-12-31
Marketing Start 2013-03-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205325
Hyphenated Format 71205-325

Supplemental Identifiers

RxCUI
351250
UPC
0371205325909
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 ANDA202389 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)
source: ndc

Packages (3)

71205-325-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30) 71205-325-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60) 71205-325-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)

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": "65ffd6fd-533b-4e39-8fbc-5c65cd88d602", "openfda": {"upc": ["0371205325909"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["1df5c652-7bad-4b07-b33b-333071bc2670"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30)", "package_ndc": "71205-325-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)", "package_ndc": "71205-325-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)", "package_ndc": "71205-325-90", "marketing_start_date": "20190901"}], "brand_name": "Escitalopram", "product_id": "71205-325_65ffd6fd-533b-4e39-8fbc-5c65cd88d602", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-325", "generic_name": "Escitalopram", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}