Package 42708-155-30

Brand: escitalopram

Generic: escitalopram
NDC Package Sample

Package Facts

Identity

Package NDC 42708-155-30
Digits Only 4270815530
Product NDC 42708-155
Product ID 42708-155_4586c105-2822-0ce2-e063-6294a90a5a72
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-155-30)

Marketing

Marketing Status
Marketed Since 2022-08-04
Brand escitalopram
Generic escitalopram
Sample Package Yes

Linked Drug Pages (1)

Escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4586c105-2822-0ce2-e063-6294a90a5a72", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["e56e8d41-188c-5a6f-e053-2a95a90a70e6"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-155-30)", "package_ndc": "42708-155-30", "marketing_start_date": "20220804"}], "brand_name": "Escitalopram", "product_id": "42708-155_4586c105-2822-0ce2-e063-6294a90a5a72", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-155", "generic_name": "Escitalopram", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}