Package 82009-138-60

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 82009-138-60
Digits Only 8200913860
Product NDC 82009-138
Product ID 82009-138_425dfa4b-ae5d-578b-e063-6394a90a4d3b
Description

1 BOTTLE in 1 CARTON (82009-138-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-06-15
Brand dimethyl fumarate
Generic dimethyl fumarate
Sample Package No

Linked Drug Pages (1)

DIMETHYL FUMARATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "425dfa4b-ae5d-578b-e063-6394a90a4d3b", "openfda": {"upc": ["0382009138602"], "unii": ["FO2303MNI2"], "rxcui": ["1373491"], "spl_set_id": ["39150ef0-ba48-4719-b7fd-9beb4d4ad3ce"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82009-138-60)  / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "82009-138-60", "marketing_start_date": "20240615"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "82009-138_425dfa4b-ae5d-578b-e063-6394a90a4d3b", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "82009-138", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210500", "marketing_category": "ANDA", "marketing_start_date": "20240615", "listing_expiration_date": "20261231"}