Package 0378-2250-05

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 0378-2250-05
Digits Only 0378225005
Product NDC 0378-2250
Description

500 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-05)

Marketing

Marketing Status
Discontinued 2026-04-30
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": "c55e1a32-db7a-4605-bab0-972a88414e7e", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058", "200060"], "spl_set_id": ["74c3a01e-9451-0f2f-6aab-8348047cb1f5"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (0378-2250-05)", "package_ndc": "0378-2250-05", "marketing_end_date": "20260430", "marketing_start_date": "20090504"}], "brand_name": "Mycophenolate Mofetil", "product_id": "0378-2250_c55e1a32-db7a-4605-bab0-972a88414e7e", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0378-2250", "generic_name": "mycophenolate mofetil", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "250 mg/1"}], "application_number": "ANDA065520", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20090504"}