Package 71288-803-92
Brand: mycophenolate mofetil
Generic: mycophenolate mofetilPackage Facts
Identity
Package NDC
71288-803-92
Digits Only
7128880392
Product NDC
71288-803
Description
4 VIAL, SINGLE-DOSE in 1 CARTON (71288-803-92) / 20 mL in 1 VIAL, SINGLE-DOSE (71288-803-91)
Marketing
Marketing Status
Brand
mycophenolate mofetil
Generic
mycophenolate mofetil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "57acc3ef-fe59-4e7b-8df3-396bdb4bb5c5", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311881"], "spl_set_id": ["b41cca9f-0922-4171-8d1b-8e0d32ae1cc1"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL, SINGLE-DOSE in 1 CARTON (71288-803-92) / 20 mL in 1 VIAL, SINGLE-DOSE (71288-803-91)", "package_ndc": "71288-803-92", "marketing_start_date": "20210115"}], "brand_name": "Mycophenolate Mofetil", "product_id": "71288-803_57acc3ef-fe59-4e7b-8df3-396bdb4bb5c5", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "71288-803", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/20mL"}], "application_number": "ANDA212130", "marketing_category": "ANDA", "marketing_start_date": "20210115", "listing_expiration_date": "20261231"}