Package 0004-0298-09
Brand: cellcept
Generic: mycophenolate mofetil hydrochloridePackage Facts
Identity
Package NDC
0004-0298-09
Digits Only
0004029809
Product NDC
0004-0298
Description
4 VIAL in 1 CARTON (0004-0298-09) / 20 mL in 1 VIAL
Marketing
Marketing Status
Brand
cellcept
Generic
mycophenolate mofetil hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ad799779-cc87-4d12-9836-74375149b84b", "openfda": {"unii": ["9242ECW6R0", "UXH81S8ZVB"], "rxcui": ["199058", "200060", "213394", "311880", "311881", "616435", "616444", "616447"], "spl_set_id": ["37241e87-4af4-4dc3-a1aa-ea6f20d8dc40"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (0004-0298-09) / 20 mL in 1 VIAL", "package_ndc": "0004-0298-09", "marketing_start_date": "19980812"}], "brand_name": "CellCept", "product_id": "0004-0298_ad799779-cc87-4d12-9836-74375149b84b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0004-0298", "generic_name": "Mycophenolate Mofetil hydrochloride", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CellCept", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL HYDROCHLORIDE", "strength": "500 mg/20mL"}], "application_number": "NDA050758", "marketing_category": "NDA", "marketing_start_date": "19980812", "listing_expiration_date": "20261231"}