escitalopram

Generic: escitalopram oxalate

Labeler: jubilant cadista pharmacuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram oxalate
Labeler jubilant cadista pharmacuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
Jubilant Cadista Pharmacuticals Inc.

Identifiers & Regulatory

Product NDC 59746-281
Product ID 59746-281_1ba045ea-2f59-4bf4-94b3-d03449c0bf77
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202280
Listing Expiration 2026-12-31
Marketing Start 2024-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59746281
Hyphenated Format 59746-281

Supplemental Identifiers

RxCUI
349332 351249 351250
UPC
0359746279103
UNII
5U85DBW7LO

Packaging Origin

Original Packager
true

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 ANDA202280 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59746-281-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (59746-281-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (59746-281-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (59746-281-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (59746-281-90)
source: ndc

Packages (5)

59746-281-01 100 TABLET, FILM COATED in 1 BOTTLE (59746-281-01) 59746-281-05 500 TABLET, FILM COATED in 1 BOTTLE (59746-281-05) 59746-281-10 1000 TABLET, FILM COATED in 1 BOTTLE (59746-281-10) 59746-281-30 30 TABLET, FILM COATED in 1 BOTTLE (59746-281-30) 59746-281-90 90 TABLET, FILM COATED in 1 BOTTLE (59746-281-90)

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": "1ba045ea-2f59-4bf4-94b3-d03449c0bf77", "openfda": {"upc": ["0359746279103"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["2db02476-325f-ee47-a7e5-b5aed56c364c"], "manufacturer_name": ["Jubilant Cadista Pharmacuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59746-281-01)", "package_ndc": "59746-281-01", "marketing_start_date": "20240101"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59746-281-05)", "package_ndc": "59746-281-05", "marketing_start_date": "20240101"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59746-281-10)", "package_ndc": "59746-281-10", "marketing_start_date": "20240101"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59746-281-30)", "package_ndc": "59746-281-30", "marketing_start_date": "20240101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59746-281-90)", "package_ndc": "59746-281-90", "marketing_start_date": "20240101"}], "brand_name": "Escitalopram", "product_id": "59746-281_1ba045ea-2f59-4bf4-94b3-d03449c0bf77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "59746-281", "generic_name": "Escitalopram Oxalate", "labeler_name": "Jubilant Cadista Pharmacuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202280", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}