escitalopram

Generic: escitalopram

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler torrent pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-137
Product ID 13668-137_aa1ecae7-8a57-434f-a72b-088335b1a42c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090939
Listing Expiration 2027-12-31
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 13668137
Hyphenated Format 13668-137

Supplemental Identifiers

RxCUI
349332 351249 351250
UPC
0313668136302 0313668137309 0313668135305
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 (source: ndc)
Application Number ANDA090939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (13668-137-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (13668-137-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (13668-137-10)
  • 2000 TABLET, FILM COATED in 1 BOTTLE (13668-137-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30)
source: ndc

Packages (5)

13668-137-01 100 TABLET, FILM COATED in 1 BOTTLE (13668-137-01) 13668-137-05 500 TABLET, FILM COATED in 1 BOTTLE (13668-137-05) 13668-137-10 1000 TABLET, FILM COATED in 1 BOTTLE (13668-137-10) 13668-137-20 2000 TABLET, FILM COATED in 1 BOTTLE (13668-137-20) 13668-137-30 30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30)

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": "aa1ecae7-8a57-434f-a72b-088335b1a42c", "openfda": {"upc": ["0313668136302", "0313668137309", "0313668135305"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["068bb338-23f3-4278-958b-c34b40456024"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (13668-137-01)", "package_ndc": "13668-137-01", "marketing_start_date": "20120911"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-137-05)", "package_ndc": "13668-137-05", "marketing_start_date": "20120911"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13668-137-10)", "package_ndc": "13668-137-10", "marketing_start_date": "20120911"}, {"sample": false, "description": "2000 TABLET, FILM COATED in 1 BOTTLE (13668-137-20)", "package_ndc": "13668-137-20", "marketing_start_date": "20120911"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-137-30)", "package_ndc": "13668-137-30", "marketing_start_date": "20120911"}], "brand_name": "escitalopram", "product_id": "13668-137_aa1ecae7-8a57-434f-a72b-088335b1a42c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "13668-137", "generic_name": "escitalopram", "labeler_name": "Torrent Pharmaceuticals Limited", "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": "20271231"}