Escitalopram

Generic: Escitalopram Oxalate

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Escitalopram
Generic Name Escitalopram Oxalate
Labeler REMEDYREPACK INC.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ESCITALOPRAM OXALATE 10 mg/1

Identifiers & Regulatory

Product NDC 70518-1103
Product ID 70518-1103_4859d5a0-7c37-17bb-e063-6394a90acce0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090432
Listing Expiration 2027-12-31
Marketing Start 2018-04-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181103
Hyphenated Format 70518-1103

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 ANDA090432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)
source: ndc

Packages (1)

70518-1103-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)

Ingredients (1)

ESCITALOPRAM OXALATE (10 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": "4859d5a0-7c37-17bb-e063-6394a90acce0", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["32780ff1-0f59-467f-b27f-e541e4c0c7d3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1103-0)", "package_ndc": "70518-1103-0", "marketing_start_date": "20180409"}], "brand_name": "Escitalopram", "product_id": "70518-1103_4859d5a0-7c37-17bb-e063-6394a90acce0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1103", "generic_name": "Escitalopram Oxalate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20180409", "listing_expiration_date": "20271231"}