escitalopram
Generic: escitalopram
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
escitalopram
Generic Name
escitalopram
Labeler
st. mary's medical park pharmacy
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
escitalopram oxalate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-894
Product ID
60760-894_3623240f-a96f-d97b-e063-6394a90a9ab6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078777
Listing Expiration
2026-12-31
Marketing Start
2023-06-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760894
Hyphenated Format
60760-894
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 (source: ndc)
Generic Name
escitalopram (source: ndc)
Application Number
ANDA078777 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-894-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3623240f-a96f-d97b-e063-6394a90a9ab6", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["362327ce-2dde-f657-e063-6394a90a0b63"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-894-30)", "package_ndc": "60760-894-30", "marketing_start_date": "20250519"}], "brand_name": "escitalopram", "product_id": "60760-894_3623240f-a96f-d97b-e063-6394a90a9ab6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-894", "generic_name": "escitalopram", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}