Package 70518-3799-0

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 70518-3799-0
Digits Only 7051837990
Product NDC 70518-3799
Description

100 POUCH in 1 BOX (70518-3799-0) / 1 CAPSULE in 1 POUCH (70518-3799-1)

Marketing

Marketing Status
Marketed Since 2023-07-18
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b2912ad-1721-3d82-e063-6394a90ad4fc", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058"], "spl_set_id": ["77a75d5b-a90d-4ee5-aa8a-6da97d130357"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3799-0)  / 1 CAPSULE in 1 POUCH (70518-3799-1)", "package_ndc": "70518-3799-0", "marketing_start_date": "20230718"}], "brand_name": "Mycophenolate mofetil", "product_id": "70518-3799_3b2912ad-1721-3d82-e063-6394a90ad4fc", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70518-3799", "generic_name": "Mycophenolate mofetil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "250 mg/1"}], "application_number": "ANDA090055", "marketing_category": "ANDA", "marketing_start_date": "20230718", "listing_expiration_date": "20261231"}