escitalopram

Generic: escitalopram

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6427
Product ID 0904-6427_6dd4eb62-4211-41c7-8592-69c0b045b53f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090939
Listing Expiration 2027-12-31
Marketing Start 2014-10-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046427
Hyphenated Format 0904-6427

Supplemental Identifiers

RxCUI
349332 351250
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 ANDA090939 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6427-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6427-61 100 BLISTER PACK in 1 CARTON (0904-6427-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

escitalopram oxalate (20 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": "6dd4eb62-4211-41c7-8592-69c0b045b53f", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["f4a12048-181e-45ed-a382-f53096d1b689"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6427-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6427-61", "marketing_start_date": "20141015"}], "brand_name": "escitalopram", "product_id": "0904-6427_6dd4eb62-4211-41c7-8592-69c0b045b53f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-6427", "generic_name": "escitalopram", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20141015", "listing_expiration_date": "20271231"}