Package 69097-322-89

Brand: dimethyl fumarate

Generic: dimethyl fumarate
NDC Package

Package Facts

Identity

Package NDC 69097-322-89
Digits Only 6909732289
Product NDC 69097-322
Description

1 BOTTLE, PLASTIC in 1 CARTON (69097-322-89) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2020-09-24
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": "d64e8be8-de52-40c2-8730-bef67c6b0914", "openfda": {"upc": ["0369097323035", "0369097322892", "0369097323882", "0369097552039"], "unii": ["FO2303MNI2"], "rxcui": ["1373483", "1373491", "1373497"], "spl_set_id": ["6c42107a-2a42-4263-97b6-ae0d7675c92a"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (69097-322-89)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "69097-322-89", "marketing_start_date": "20200924"}], "brand_name": "DIMETHYL FUMARATE", "product_id": "69097-322_d64e8be8-de52-40c2-8730-bef67c6b0914", "dosage_form": "CAPSULE, DELAYED RELEASE", "product_ndc": "69097-322", "generic_name": "DIMETHYL FUMARATE", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIMETHYL FUMARATE", "active_ingredients": [{"name": "DIMETHYL FUMARATE", "strength": "120 mg/1"}], "application_number": "ANDA210305", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}