Package 70377-040-11

Brand: mycophenolic acid

Generic: mycophenolic acid
NDC Package

Package Facts

Identity

Package NDC 70377-040-11
Digits Only 7037704011
Product NDC 70377-040
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (70377-040-11)

Marketing

Marketing Status
Marketed Since 2022-05-30
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": "c88acb03-1331-2837-85be-e4de5c5ad539", "openfda": {"upc": ["0370377040115"], "unii": ["WX877SQI1G"], "rxcui": ["485020", "485023"], "spl_set_id": ["8516e135-5cc0-ef2d-6dad-0f9f841bb27b"], "manufacturer_name": ["Biocon Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (70377-040-11)", "package_ndc": "70377-040-11", "marketing_start_date": "20220530"}], "brand_name": "Mycophenolic Acid", "product_id": "70377-040_c88acb03-1331-2837-85be-e4de5c5ad539", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70377-040", "generic_name": "Mycophenolic Acid", "labeler_name": "Biocon Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolic Acid", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "360 mg/1"}], "application_number": "ANDA214630", "marketing_category": "ANDA", "marketing_start_date": "20220530", "listing_expiration_date": "20261231"}