Package 70771-1530-7

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package Sample

Package Facts

Identity

Package NDC 70771-1530-7
Digits Only 7077115307
Product NDC 70771-1530
Product ID 70771-1530_d8dceb92-b903-4b29-b3e6-4651fbc598fe
Description

14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)

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": "d8dceb92-b903-4b29-b3e6-4651fbc598fe", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["7203a262-de0f-42dd-b4fb-8856758b82e9"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1530-7)", "package_ndc": "70771-1530-7", "marketing_start_date": "20200928"}], "brand_name": "dimethyl fumarate", "product_id": "70771-1530_d8dceb92-b903-4b29-b3e6-4651fbc598fe", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "70771-1530", "generic_name": "dimethyl fumarate", "labeler_name": "Zydus Lifesciences Limited", "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"}