escitalopram oxalate

Generic: escitalopram oxalate

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram oxalate
Labeler northstar rxllc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/21

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-151
Product ID 72603-151_cb888b2f-8092-43a1-8542-a10e2b004369
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202210
Listing Expiration 2026-12-31
Marketing Start 2024-01-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603151
Hyphenated Format 72603-151

Supplemental Identifiers

RxCUI
349332 351249 351250
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 oxalate (source: ndc)
Generic Name escitalopram oxalate (source: ndc)
Application Number ANDA202210 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/21
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72603-151-01)
source: ndc

Packages (1)

72603-151-01 1000 TABLET, FILM COATED in 1 BOTTLE (72603-151-01)

Ingredients (1)

escitalopram oxalate (20 mg/21)

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cb888b2f-8092-43a1-8542-a10e2b004369", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["81840aec-96fd-4af2-bd10-3f38d068f39a"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72603-151-01)", "package_ndc": "72603-151-01", "marketing_start_date": "20240108"}], "brand_name": "Escitalopram Oxalate", "product_id": "72603-151_cb888b2f-8092-43a1-8542-a10e2b004369", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72603-151", "generic_name": "Escitalopram Oxalate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/21"}], "application_number": "ANDA202210", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}