escitalopram

Generic: escitalopram

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler st. mary's medical park pharmacy
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-895
Product ID 60760-895_47d4373f-7797-2ab5-e063-6294a90a40c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078777
Listing Expiration 2027-12-31
Marketing Start 2023-06-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760895
Hyphenated Format 60760-895

Supplemental Identifiers

RxCUI
349332
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 (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number ANDA078777 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)
source: ndc

Packages (2)

60760-895-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-30) 60760-895-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)

Ingredients (1)

escitalopram oxalate (10 mg/1)

Linked Drug Pages (1)

escitalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d4373f-7797-2ab5-e063-6294a90a40c4", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["1b2ec266-be5b-9265-e063-6294a90a10e3"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-30)", "package_ndc": "60760-895-30", "marketing_start_date": "20250513"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-895-90)", "package_ndc": "60760-895-90", "marketing_start_date": "20240612"}], "brand_name": "escitalopram", "product_id": "60760-895_47d4373f-7797-2ab5-e063-6294a90a40c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-895", "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": "10 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20271231"}