Package 72189-449-30

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 72189-449-30
Digits Only 7218944930
Product NDC 72189-449
Product ID 72189-449_2c4db59b-4a03-c45c-e063-6294a90ab0ff
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-449-30)

Marketing

Marketing Status
Marketed Since 2023-03-20
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": "2c4db59b-4a03-c45c-e063-6294a90ab0ff", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["f75aabf8-f4a1-acd1-e053-6294a90ab9a6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-449-30)", "package_ndc": "72189-449-30", "marketing_start_date": "20230320"}], "brand_name": "Escitalopram", "product_id": "72189-449_2c4db59b-4a03-c45c-e063-6294a90ab0ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-449", "generic_name": "Escitalopram", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20230320", "listing_expiration_date": "20261231"}