Package 59651-621-08

Brand: mycophenolic acid

Generic: mycophenolic acid
NDC Package

Package Facts

Identity

Package NDC 59651-621-08
Digits Only 5965162108
Product NDC 59651-621
Product ID 59651-621_f6e5e3de-bd8c-451a-a6f0-831b15ede576
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-621-08)

Marketing

Marketing Status
Marketed Since 2024-02-27
Brand mycophenolic acid
Generic mycophenolic acid
Sample Package No

Linked Drug Pages (1)

MYCOPHENOLIC ACID ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6e5e3de-bd8c-451a-a6f0-831b15ede576", "openfda": {"unii": ["WX877SQI1G"], "rxcui": ["485020", "485023"], "spl_set_id": ["5b224d7f-fecb-4531-9d27-008347777c9d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (59651-621-08)", "package_ndc": "59651-621-08", "marketing_start_date": "20240227"}], "brand_name": "MYCOPHENOLIC ACID", "product_id": "59651-621_f6e5e3de-bd8c-451a-a6f0-831b15ede576", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "59651-621", "generic_name": "MYCOPHENOLIC ACID", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MYCOPHENOLIC ACID", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "180 mg/1"}], "application_number": "ANDA218603", "marketing_category": "ANDA", "marketing_start_date": "20240227", "listing_expiration_date": "20261231"}