Package 33342-350-95

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 33342-350-95
Digits Only 3334235095
Product NDC 33342-350
Description

46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-350-95)

Marketing

Marketing Status
Marketed Since 2025-06-27
Brand dimethyl fumarate
Generic dimethyl fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef3e9cf5-b172-4e67-b621-dc94e9e9d93f", "openfda": {"upc": ["0333342349095"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["f8ada3e3-55c0-43e3-95b9-c6d11ffc42dd"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-350-09)", "package_ndc": "33342-350-09", "marketing_start_date": "20240626"}, {"sample": false, "description": "46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-350-95)", "package_ndc": "33342-350-95", "marketing_start_date": "20250627"}], "brand_name": "Dimethyl Fumarate", "product_id": "33342-350_ef3e9cf5-b172-4e67-b621-dc94e9e9d93f", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "33342-350", "generic_name": "Dimethyl Fumarate", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimethyl Fumarate", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "240 mg/1"}], "application_number": "ANDA210377", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}