Package 82249-747-60

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 82249-747-60
Digits Only 8224974760
Product NDC 82249-747
Product ID 82249-747_ca6c6bda-05ac-4a39-8356-86bdfa61e863
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (82249-747-60)

Marketing

Marketing Status
Marketed Since 2025-06-11
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": "ca6c6bda-05ac-4a39-8356-86bdfa61e863", "openfda": {"upc": ["0382249747602"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491"], "spl_set_id": ["f3002b6a-841e-4247-9155-3acfb30cabcd"], "manufacturer_name": ["CivicaScript LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (82249-747-60)", "package_ndc": "82249-747-60", "marketing_start_date": "20250611"}], "brand_name": "Dimethyl fumarate", "product_id": "82249-747_ca6c6bda-05ac-4a39-8356-86bdfa61e863", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "82249-747", "generic_name": "Dimethyl fumarate", "labeler_name": "CivicaScript LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210440", "marketing_category": "ANDA", "marketing_start_date": "20250611", "listing_expiration_date": "20261231"}