Package 42023-172-04

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 42023-172-04
Digits Only 4202317204
Product NDC 42023-172
Product ID 42023-172_4014ae09-3242-4e13-abf1-62645c181001
Description

4 VIAL in 1 CARTON (42023-172-04) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2016-10-28
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Mycophenolate Mofetil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4014ae09-3242-4e13-abf1-62645c181001", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311881"], "spl_set_id": ["35ba0428-e267-49a5-99a9-c58853f7989d"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (42023-172-04)  / 20 mL in 1 VIAL", "package_ndc": "42023-172-04", "marketing_start_date": "20161028"}], "brand_name": "Mycophenolate Mofetil", "product_id": "42023-172_4014ae09-3242-4e13-abf1-62645c181001", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "42023-172", "generic_name": "mycophenolate mofetil", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/20mL"}], "application_number": "ANDA203575", "marketing_category": "ANDA", "marketing_start_date": "20161028", "listing_expiration_date": "20261231"}