Package 72789-194-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 72789-194-90
Digits Only 7278919490
Product NDC 72789-194
Product ID 72789-194_4b0835eb-6098-311e-e063-6394a90a3fae
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-194-90)

Marketing

Marketing Status
Marketed Since 2021-06-14
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": "4b0835eb-6098-311e-e063-6394a90a3fae", "openfda": {"upc": ["0372789194905"], "unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["83510549-bd47-4969-aba0-c149a0fbb7f3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-194-30)", "package_ndc": "72789-194-30", "marketing_start_date": "20210622"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-194-90)", "package_ndc": "72789-194-90", "marketing_start_date": "20210614"}], "brand_name": "Escitalopram", "product_id": "72789-194_4b0835eb-6098-311e-e063-6394a90a3fae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-194", "generic_name": "Escitalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA202389", "marketing_category": "ANDA", "marketing_start_date": "20130319", "listing_expiration_date": "20271231"}