Package 72189-438-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 72189-438-90
Digits Only 7218943890
Product NDC 72189-438
Product ID 72189-438_2c4d7dfd-fbd4-516b-e063-6394a90add1b
Description

90 TABLET in 1 BOTTLE (72189-438-90)

Marketing

Marketing Status
Marketed Since 2023-03-13
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": "2c4d7dfd-fbd4-516b-e063-6394a90add1b", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["f6cacd68-0f55-deb9-e053-6294a90aa266"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-438-30)", "package_ndc": "72189-438-30", "marketing_start_date": "20230313"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-438-90)", "package_ndc": "72189-438-90", "marketing_start_date": "20230313"}], "brand_name": "Escitalopram", "product_id": "72189-438_2c4d7dfd-fbd4-516b-e063-6394a90add1b", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-438", "generic_name": "Escitalopram", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20261231"}