escitalopram

Generic: escitalopram

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

Drug Facts

Product Profile

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

escitalopram oxalate 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4239
Product ID 70518-4239_38f3e618-59de-4504-e063-6394a90afa55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078777
Listing Expiration 2026-12-31
Marketing Start 2024-12-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184239
Hyphenated Format 70518-4239

Supplemental Identifiers

RxCUI
351250
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 ANDA078777 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1)
  • 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)
source: ndc

Packages (4)

70518-4239-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0) 70518-4239-1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1) 70518-4239-2 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2) 70518-4239-3 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)

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": "38f3e618-59de-4504-e063-6394a90afa55", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["53a7e974-9945-4e42-8395-b567bf9f1c4e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4239-0)", "package_ndc": "70518-4239-0", "marketing_start_date": "20241213"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-1)", "package_ndc": "70518-4239-1", "marketing_start_date": "20250225"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-2)", "package_ndc": "70518-4239-2", "marketing_start_date": "20250619"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)", "package_ndc": "70518-4239-3", "marketing_start_date": "20250701"}], "brand_name": "escitalopram", "product_id": "70518-4239_38f3e618-59de-4504-e063-6394a90afa55", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4239", "generic_name": "escitalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20241213", "listing_expiration_date": "20261231"}