escitalopram

Generic: escitalopram

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

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3069
Product ID 68071-3069_1d8e7443-eb23-ccda-e063-6394a90ae343
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 680713069
Hyphenated Format 68071-3069

Supplemental Identifiers

RxCUI
351250
UPC
0368071306934
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 (68071-3069-3)
  • 28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)
source: ndc

Packages (2)

68071-3069-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3) 68071-3069-8 28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)

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": "1d8e7443-eb23-ccda-e063-6394a90ae343", "openfda": {"upc": ["0368071306934"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["4a645652-ae1f-3811-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3069-3)", "package_ndc": "68071-3069-3", "marketing_start_date": "20170310"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68071-3069-8)", "package_ndc": "68071-3069-8", "marketing_start_date": "20170310"}], "brand_name": "Escitalopram", "product_id": "68071-3069_1d8e7443-eb23-ccda-e063-6394a90ae343", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3069", "generic_name": "Escitalopram", "labeler_name": "NuCare Pharmaceuticals, 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"}