Package 71205-782-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71205-782-90
Digits Only 7120578290
Product NDC 71205-782
Product ID 71205-782_3e3de8ea-b96b-456b-9336-69380fd2d058
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-782-90)

Marketing

Marketing Status
Marketed Since 2023-03-28
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": "3e3de8ea-b96b-456b-9336-69380fd2d058", "openfda": {"upc": ["0371205782900"], "unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["3e3de8ea-b96b-456b-9336-69380fd2d058"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-782-30)", "package_ndc": "71205-782-30", "marketing_start_date": "20230328"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-782-60)", "package_ndc": "71205-782-60", "marketing_start_date": "20230328"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-782-90)", "package_ndc": "71205-782-90", "marketing_start_date": "20230328"}], "brand_name": "Escitalopram", "product_id": "71205-782_3e3de8ea-b96b-456b-9336-69380fd2d058", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-782", "generic_name": "Escitalopram", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}