Package 70512-852-14

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 70512-852-14
Digits Only 7051285214
Product NDC 70512-852
Product ID 70512-852_457243f3-2d22-3222-e063-6394a90ae21e
Description

1 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-03-12
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": "457243f3-2d22-3222-e063-6394a90ae21e", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491"], "spl_set_id": ["b4a200c1-f25a-4aa8-8770-06182fdeda9d"], "manufacturer_name": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70512-852-14)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "70512-852-14", "marketing_start_date": "20230312"}], "brand_name": "Dimethyl Fumarate", "product_id": "70512-852_457243f3-2d22-3222-e063-6394a90ae21e", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "70512-852", "generic_name": "Dimethyl Fumarate", "labeler_name": "SOLA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl Fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210436", "marketing_category": "ANDA", "marketing_start_date": "20230131", "listing_expiration_date": "20261231"}