Package 71335-2960-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71335-2960-1
Digits Only 7133529601
Product NDC 71335-2960
Product ID 71335-2960_11428fb6-bdb0-48ae-8e46-e2816dd13408
Description

1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)

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": "11428fb6-bdb0-48ae-8e46-e2816dd13408", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["1d2f83c1-8ffe-48f3-a084-150289001743"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)", "package_ndc": "71335-2960-1", "marketing_start_date": "20251022"}], "brand_name": "escitalopram", "product_id": "71335-2960_11428fb6-bdb0-48ae-8e46-e2816dd13408", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2960", "generic_name": "escitalopram", "labeler_name": "Bryant Ranch Prepack", "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": "20120911", "listing_expiration_date": "20261231"}