Package 43598-430-60

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 43598-430-60
Digits Only 4359843060
Product NDC 43598-430
Product ID 43598-430_fcfea8cf-7720-664c-345c-b8baeff438ee
Description

1 BOTTLE in 1 CARTON (43598-430-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-09-25
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": "fcfea8cf-7720-664c-345c-b8baeff438ee", "openfda": {"unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491"], "spl_set_id": ["b00dcf89-59d3-9ab2-fd9b-16b9ec2d677b"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-430-60)  / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "43598-430-60", "marketing_start_date": "20200925"}], "brand_name": "Dimethyl Fumarate", "product_id": "43598-430_fcfea8cf-7720-664c-345c-b8baeff438ee", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "43598-430", "generic_name": "Dimethyl fumarate", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl Fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210460", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20261231"}