Package 71335-2903-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71335-2903-1
Digits Only 7133529031
Product NDC 71335-2903
Product ID 71335-2903_72212dba-b9a9-4385-972c-9f6300227a1e
Description

1000 TABLET, FILM COATED in 1 BOTTLE (71335-2903-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "72212dba-b9a9-4385-972c-9f6300227a1e", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["5c00c4d3-8248-4321-adec-03886c0d0f7b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-2903-1)", "package_ndc": "71335-2903-1", "marketing_start_date": "20251022"}], "brand_name": "escitalopram", "product_id": "71335-2903_72212dba-b9a9-4385-972c-9f6300227a1e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2903", "generic_name": "escitalopram", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}