Package 0078-0386-66

Brand: myfortic

Generic: mycophenolic acid
NDC Package

Package Facts

Identity

Package NDC 0078-0386-66
Digits Only 0078038666
Product NDC 0078-0386
Product ID 0078-0386_c5665f04-bf64-4cc7-b98b-171a8f57155b
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (0078-0386-66)

Marketing

Marketing Status
Marketed Since 2004-02-27
Brand myfortic
Generic mycophenolic acid
Sample Package No

Linked Drug Pages (1)

Myfortic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c5665f04-bf64-4cc7-b98b-171a8f57155b", "openfda": {"upc": ["0300780386661"], "unii": ["WX877SQI1G"], "rxcui": ["485020", "485023", "616449", "616450"], "spl_set_id": ["eed26501-890d-4ff6-88e7-6dbea4726e53"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (0078-0386-66)", "package_ndc": "0078-0386-66", "marketing_start_date": "20040227"}], "brand_name": "Myfortic", "product_id": "0078-0386_c5665f04-bf64-4cc7-b98b-171a8f57155b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0078-0386", "generic_name": "mycophenolic acid", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Myfortic", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "360 mg/1"}], "application_number": "NDA050791", "marketing_category": "NDA", "marketing_start_date": "20040227", "listing_expiration_date": "20261231"}