escitalopram

Generic: escitalopram

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler redpharm drug, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1421
Product ID 67296-1421_2c6228e2-dbab-01e7-e063-6394a90acbbc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078032
Listing Expiration 2026-12-31
Marketing Start 2012-03-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672961421
Hyphenated Format 67296-1421

Supplemental Identifiers

RxCUI
351250
UPC
0367296142174
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 ANDA078032 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)
source: ndc

Packages (1)

67296-1421-3 30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)

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": "2c6228e2-dbab-01e7-e063-6394a90acbbc", "openfda": {"upc": ["0367296142174"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["fc61822a-4058-343c-e053-6294a90af72c"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)", "package_ndc": "67296-1421-3", "marketing_start_date": "20210201"}], "brand_name": "Escitalopram", "product_id": "67296-1421_2c6228e2-dbab-01e7-e063-6394a90acbbc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "67296-1421", "generic_name": "Escitalopram", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}