escitalopram oxalate
Generic: escitalopram oxalate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
escitalopram oxalate
Generic Name
escitalopram oxalate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
escitalopram oxalate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2242
Product ID
72162-2242_a3f1acbc-6b69-4ce6-95a7-e51a2023ea50
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090939
Listing Expiration
2026-12-31
Marketing Start
2012-09-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622242
Hyphenated Format
72162-2242
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE (72162-2242-0)
- 100 TABLET in 1 BOTTLE (72162-2242-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a3f1acbc-6b69-4ce6-95a7-e51a2023ea50", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["a0ff752d-cb30-4131-a7d6-cd66d8a47b1a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2242-0)", "package_ndc": "72162-2242-0", "marketing_start_date": "20120911"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2242-1)", "package_ndc": "72162-2242-1", "marketing_start_date": "20120911"}], "brand_name": "escitalopram oxalate", "product_id": "72162-2242_a3f1acbc-6b69-4ce6-95a7-e51a2023ea50", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2242", "generic_name": "escitalopram oxalate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}