Package 70710-1204-7

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package Sample

Package Facts

Identity

Package NDC 70710-1204-7
Digits Only 7071012047
Product NDC 70710-1204
Product ID 70710-1204_548169c7-23fb-46e1-9a8d-556a00ee5cbc
Description

14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1204-7)

Marketing

Marketing Status
Marketed Since 2020-09-28
Brand dimethyl fumarate
Generic dimethyl fumarate
Sample Package Yes

Linked Drug Pages (1)

dimethyl fumarate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "548169c7-23fb-46e1-9a8d-556a00ee5cbc", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["e7ef9b9e-d97a-4a56-b792-a1a255613156"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1204-7)", "package_ndc": "70710-1204-7", "marketing_start_date": "20200928"}], "brand_name": "dimethyl fumarate", "product_id": "70710-1204_548169c7-23fb-46e1-9a8d-556a00ee5cbc", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "70710-1204", "generic_name": "dimethyl fumarate", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dimethyl fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210538", "marketing_category": "ANDA", "marketing_start_date": "20200928", "listing_expiration_date": "20261231"}