Package 71288-803-21

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 71288-803-21
Digits Only 7128880321
Product NDC 71288-803
Description

4 VIAL, SINGLE-DOSE in 1 CARTON (71288-803-21) / 20 mL in 1 VIAL, SINGLE-DOSE (71288-803-20)

Marketing

Marketing Status
Marketed Since 2021-01-15
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": "39b278d4-58de-4a14-a73f-4682305a90f5", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311881"], "spl_set_id": ["9650af9b-d36f-4a2f-9647-d0f798933402"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL, SINGLE-DOSE in 1 CARTON (71288-803-21)  / 20 mL in 1 VIAL, SINGLE-DOSE (71288-803-20)", "package_ndc": "71288-803-21", "marketing_start_date": "20210115"}], "brand_name": "Mycophenolate Mofetil", "product_id": "71288-803_39b278d4-58de-4a14-a73f-4682305a90f5", "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"}