Package 67296-1421-3

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 67296-1421-3
Digits Only 6729614213
Product NDC 67296-1421
Product ID 67296-1421_2c6228e2-dbab-01e7-e063-6394a90acbbc
Description

30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)

Marketing

Marketing Status
Marketed Since 2021-02-01
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": "2c6228e2-dbab-01e7-e063-6394a90acbbc", "openfda": {"upc": ["0367296142174"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["fc61822a-4058-343c-e053-6294a90af72c"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-1421-3)", "package_ndc": "67296-1421-3", "marketing_start_date": "20210201"}], "brand_name": "Escitalopram", "product_id": "67296-1421_2c6228e2-dbab-01e7-e063-6394a90acbbc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "67296-1421", "generic_name": "Escitalopram", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20120315", "listing_expiration_date": "20261231"}