Package 10702-278-03

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 10702-278-03
Digits Only 1070227803
Product NDC 10702-278
Product ID 10702-278_3843c448-c1bf-a403-e063-6394a90a3e77
Description

30 TABLET in 1 BOTTLE (10702-278-03)

Marketing

Marketing Status
Marketed Since 2020-07-23
Brand leflunomide
Generic leflunomide
Sample Package No

Linked Drug Pages (1)

Leflunomide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3843c448-c1bf-a403-e063-6394a90a3e77", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["a48e6ef2-48ad-4fcf-9e67-dbba83ab0b79"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-278-03)", "package_ndc": "10702-278-03", "marketing_start_date": "20200723"}], "brand_name": "Leflunomide", "product_id": "10702-278_3843c448-c1bf-a403-e063-6394a90a3e77", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "10702-278", "generic_name": "Leflunomide", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA212453", "marketing_category": "ANDA", "marketing_start_date": "20200723", "listing_expiration_date": "20261231"}