Package 60505-2965-7

Brand: mycophenolic acid

Generic: mycophenolic acid
NDC Package

Package Facts

Identity

Package NDC 60505-2965-7
Digits Only 6050529657
Product NDC 60505-2965
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-7)

Marketing

Marketing Status
Marketed Since 2012-08-21
Brand mycophenolic acid
Generic mycophenolic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fa09fa75-fabc-fac1-8b3e-772bcf55939a", "openfda": {"unii": ["WX877SQI1G"], "rxcui": ["485020", "485023"], "spl_set_id": ["c0efafa6-d249-f44a-fbf3-e6bd3acaf6f0"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (60505-2965-7)", "package_ndc": "60505-2965-7", "marketing_start_date": "20120821"}], "brand_name": "Mycophenolic Acid", "product_id": "60505-2965_fa09fa75-fabc-fac1-8b3e-772bcf55939a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "60505-2965", "generic_name": "Mycophenolic Acid", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolic Acid", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "180 mg/1"}], "application_number": "ANDA091558", "marketing_category": "ANDA", "marketing_start_date": "20120821", "listing_expiration_date": "20261231"}