escitalopram oxalate

Generic: escitalopram oxalate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram oxalate
Labeler rising pharma holdings, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

escitalopram oxalate 5 mg/5mL

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-769
Product ID 16571-769_abf4fee5-eae0-4b5c-8b7d-7d055d36e530
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079062
Listing Expiration 2026-12-31
Marketing Start 2012-04-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571769
Hyphenated Format 16571-769

Supplemental Identifiers

RxCUI
351285
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 ANDA079062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 240 mL in 1 BOTTLE (16571-769-24)
source: ndc

Packages (1)

16571-769-24 240 mL in 1 BOTTLE (16571-769-24)

Ingredients (1)

escitalopram oxalate (5 mg/5mL)

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "abf4fee5-eae0-4b5c-8b7d-7d055d36e530", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["79fddc2d-2dc2-444f-8fd3-0337090ee744"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (16571-769-24)", "package_ndc": "16571-769-24", "marketing_start_date": "20120403"}], "brand_name": "Escitalopram Oxalate", "product_id": "16571-769_abf4fee5-eae0-4b5c-8b7d-7d055d36e530", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16571-769", "generic_name": "Escitalopram Oxalate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA079062", "marketing_category": "ANDA", "marketing_start_date": "20120403", "listing_expiration_date": "20261231"}