Package 59651-084-60

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 59651-084-60
Digits Only 5965108460
Product NDC 59651-084
Product ID 59651-084_4d4ea332-4695-4c8c-ba54-c6e24fdee31c
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-084-60)

Marketing

Marketing Status
Marketed Since 2022-12-22
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": "4d4ea332-4695-4c8c-ba54-c6e24fdee31c", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491"], "spl_set_id": ["08f3a987-6571-42b3-854b-186d782b4494"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-084-60)", "package_ndc": "59651-084-60", "marketing_start_date": "20221222"}], "brand_name": "Dimethyl Fumarate", "product_id": "59651-084_4d4ea332-4695-4c8c-ba54-c6e24fdee31c", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "59651-084", "generic_name": "Dimethyl Fumarate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl Fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210385", "marketing_category": "ANDA", "marketing_start_date": "20221222", "listing_expiration_date": "20261231"}