Package 43547-024-14

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 43547-024-14
Digits Only 4354702414
Product NDC 43547-024
Product ID 43547-024_870120b7-7d68-4e5f-98cc-ac646624feb4
Description

14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43547-024-14)

Marketing

Marketing Status
Marketed Since 2022-10-18
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": "870120b7-7d68-4e5f-98cc-ac646624feb4", "openfda": {"upc": ["0343547025069", "0343547024147"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491"], "spl_set_id": ["a3677dce-a44b-481f-8a76-9ff3a4d42105"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43547-024-14)", "package_ndc": "43547-024-14", "marketing_start_date": "20221018"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "43547-024_870120b7-7d68-4e5f-98cc-ac646624feb4", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "43547-024", "generic_name": "dimethyl fumarate", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210414", "marketing_category": "ANDA", "marketing_start_date": "20221018", "listing_expiration_date": "20261231"}