Package 13668-135-01

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 13668-135-01
Digits Only 1366813501
Product NDC 13668-135
Description

100 TABLET, FILM COATED in 1 BOTTLE (13668-135-01)

Marketing

Marketing Status
Marketed Since 2012-09-11
Brand escitalopram
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aa1ecae7-8a57-434f-a72b-088335b1a42c", "openfda": {"upc": ["0313668136302", "0313668137309", "0313668135305"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["068bb338-23f3-4278-958b-c34b40456024"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (13668-135-01)", "package_ndc": "13668-135-01", "marketing_start_date": "20120911"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-135-05)", "package_ndc": "13668-135-05", "marketing_start_date": "20120911"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13668-135-10)", "package_ndc": "13668-135-10", "marketing_start_date": "20120911"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-135-30)", "package_ndc": "13668-135-30", "marketing_start_date": "20120911"}, {"sample": false, "description": "4000 TABLET, FILM COATED in 1 BOTTLE (13668-135-40)", "package_ndc": "13668-135-40", "marketing_start_date": "20120911"}], "brand_name": "escitalopram", "product_id": "13668-135_aa1ecae7-8a57-434f-a72b-088335b1a42c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "13668-135", "generic_name": "escitalopram", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20271231"}