Package 83270-000-04

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 83270-000-04
Digits Only 8327000004
Product NDC 83270-000
Description

4 VIAL in 1 CARTON (83270-000-04) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-04-30
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "42ed2be4-bc3d-281a-e063-6394a90aeb7f", "openfda": {"upc": ["0383270000018"], "unii": ["9242ECW6R0"], "rxcui": ["311881"], "spl_set_id": ["461a252f-ff81-4e08-b256-a497b14835fa"], "manufacturer_name": ["ONESOURCE SPECIALTY PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (83270-000-04)  / 20 mL in 1 VIAL", "package_ndc": "83270-000-04", "marketing_start_date": "20230430"}], "brand_name": "mycophenolate mofetil", "product_id": "83270-000_42ed2be4-bc3d-281a-e063-6394a90aeb7f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "83270-000", "generic_name": "mycophenolate mofetil", "labeler_name": "ONESOURCE SPECIALTY PHARMA LIMITED", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/20mL"}], "application_number": "ANDA216390", "marketing_category": "ANDA", "marketing_start_date": "20230430", "listing_expiration_date": "20261231"}