escitalopram oxalate

Generic: escitalopram oxalate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram oxalate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-761
Product ID 43063-761_419e34ea-17b4-ec32-e063-6394a90a603d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090939
Listing Expiration 2026-12-31
Marketing Start 2012-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063761
Hyphenated Format 43063-761

Supplemental Identifiers

RxCUI
349332
UPC
0343063761304
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 oxalate (source: ndc)
Generic Name escitalopram oxalate (source: ndc)
Application Number ANDA090939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-01)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90)
source: ndc

Packages (3)

43063-761-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-01) 43063-761-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30) 43063-761-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90)

Ingredients (1)

escitalopram oxalate (10 mg/1)

Linked Drug Pages (1)

escitalopram oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "419e34ea-17b4-ec32-e063-6394a90a603d", "openfda": {"upc": ["0343063761304"], "unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["b7670e51-8f44-4f64-b110-3f2f431a4032"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-01)", "package_ndc": "43063-761-01", "marketing_start_date": "20170525"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-30)", "package_ndc": "43063-761-30", "marketing_start_date": "20170525"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-761-90)", "package_ndc": "43063-761-90", "marketing_start_date": "20170503"}], "brand_name": "escitalopram oxalate", "product_id": "43063-761_419e34ea-17b4-ec32-e063-6394a90a603d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-761", "generic_name": "escitalopram oxalate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}