Package 70436-172-23
Brand: mycophenolic acid
Generic: mycophenolic acidPackage Facts
Identity
Package NDC
70436-172-23
Digits Only
7043617223
Product NDC
70436-172
Description
120 TABLET, DELAYED RELEASE in 1 BOTTLE (70436-172-23)
Marketing
Marketing Status
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": "1b38818e-0b2a-d949-e063-6294a90a1129", "openfda": {"upc": ["0370436173235", "0370436172238"], "unii": ["WX877SQI1G"], "rxcui": ["485020", "485023"], "spl_set_id": ["c1ce92ef-4102-1487-e053-2995a90ac521"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (70436-172-23)", "package_ndc": "70436-172-23", "marketing_start_date": "20210519"}], "brand_name": "Mycophenolic Acid", "product_id": "70436-172_1b38818e-0b2a-d949-e063-6294a90a1129", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70436-172", "generic_name": "Mycophenolic Acid", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolic Acid", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "180 mg/1"}], "application_number": "ANDA214376", "marketing_category": "ANDA", "marketing_start_date": "20210519", "listing_expiration_date": "20261231"}