Package 71335-2460-1

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71335-2460-1
Digits Only 7133524601
Product NDC 71335-2460
Product ID 71335-2460_8ce8cbca-a1cc-455c-86e1-03a698d5f0d4
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2460-1)

Marketing

Marketing Status
Marketed Since 2024-09-27
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": "8ce8cbca-a1cc-455c-86e1-03a698d5f0d4", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["3ca5da44-403b-4c9f-9dde-f5a87866836d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2460-1)", "package_ndc": "71335-2460-1", "marketing_start_date": "20240927"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2460-2)", "package_ndc": "71335-2460-2", "marketing_start_date": "20241212"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2460-3)", "package_ndc": "71335-2460-3", "marketing_start_date": "20240729"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2460-4)", "package_ndc": "71335-2460-4", "marketing_start_date": "20241212"}], "brand_name": "escitalopram", "product_id": "71335-2460_8ce8cbca-a1cc-455c-86e1-03a698d5f0d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2460", "generic_name": "escitalopram", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}