Package 71205-325-60

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 71205-325-60
Digits Only 7120532560
Product NDC 71205-325
Product ID 71205-325_65ffd6fd-533b-4e39-8fbc-5c65cd88d602
Description

60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)

Marketing

Marketing Status
Marketed Since 2019-09-01
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": "65ffd6fd-533b-4e39-8fbc-5c65cd88d602", "openfda": {"upc": ["0371205325909"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["1df5c652-7bad-4b07-b33b-333071bc2670"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-325-30)", "package_ndc": "71205-325-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-325-60)", "package_ndc": "71205-325-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)", "package_ndc": "71205-325-90", "marketing_start_date": "20190901"}], "brand_name": "Escitalopram", "product_id": "71205-325_65ffd6fd-533b-4e39-8fbc-5c65cd88d602", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-325", "generic_name": "Escitalopram", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130321", "listing_expiration_date": "20261231"}