escitalopram

Generic: escitalopram

Labeler: accord healthcare inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/1

Manufacturer
Accord Healthcare Inc.

Identifiers & Regulatory

Product NDC 16729-170
Product ID 16729-170_411f7056-e508-9e1b-e063-6294a90a6396
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 16729170
Hyphenated Format 16729-170

Supplemental Identifiers

RxCUI
349332 351249 351250
UPC
0316729170109 0316729169103 0316729168106
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 ANDA202389 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)
source: ndc

Packages (2)

16729-170-01 100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01) 16729-170-17 1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)

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": "411f7056-e508-9e1b-e063-6294a90a6396", "openfda": {"upc": ["0316729170109", "0316729169103", "0316729168106"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["84b2028d-eff4-434d-b71e-6a3c0812f625"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16729-170-01)", "package_ndc": "16729-170-01", "marketing_start_date": "20130321"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)", "package_ndc": "16729-170-17", "marketing_start_date": "20131112"}], "brand_name": "Escitalopram", "product_id": "16729-170_411f7056-e508-9e1b-e063-6294a90a6396", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16729-170", "generic_name": "Escitalopram", "labeler_name": "Accord Healthcare Inc.", "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"}