Package 70518-4036-0

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 70518-4036-0
Digits Only 7051840360
Product NDC 70518-4036
Description

100 POUCH in 1 BOX (70518-4036-0) / 1 CAPSULE in 1 POUCH (70518-4036-1)

Marketing

Marketing Status
Marketed Since 2024-03-11
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": "3f9fc1fe-87b8-a8cf-e063-6394a90a2c38", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058"], "spl_set_id": ["d203775c-bf36-460c-bacf-3ab2348a514f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4036-0)  / 1 CAPSULE in 1 POUCH (70518-4036-1)", "package_ndc": "70518-4036-0", "marketing_start_date": "20240311"}], "brand_name": "MYCOPHENOLATE MOFETIL", "product_id": "70518-4036_3f9fc1fe-87b8-a8cf-e063-6394a90a2c38", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70518-4036", "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": "ANDA210181", "marketing_category": "ANDA", "marketing_start_date": "20240311", "listing_expiration_date": "20261231"}