Package 54288-141-04

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54288-141-04
Digits Only 5428814104
Product NDC 54288-141
Product ID 54288-141_1a8abd3a-6834-4468-a443-ca95e795b17d
Description

4 VIAL in 1 CARTON (54288-141-04) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-03-08
Brand mycophenolate mofetil
Generic mycophenolate mofetil hydrochloride
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": "1a8abd3a-6834-4468-a443-ca95e795b17d", "openfda": {"upc": ["0354288141017", "0354288141048"], "unii": ["UXH81S8ZVB"], "rxcui": ["311881"], "spl_set_id": ["32001417-130d-4c08-8e63-94ba3627ce5f"], "manufacturer_name": ["BPI Labs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 VIAL in 1 CARTON (54288-141-04)  / 20 mL in 1 VIAL", "package_ndc": "54288-141-04", "marketing_start_date": "20230308"}], "brand_name": "Mycophenolate Mofetil", "product_id": "54288-141_1a8abd3a-6834-4468-a443-ca95e795b17d", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "54288-141", "generic_name": "Mycophenolate Mofetil hydrochloride", "labeler_name": "BPI Labs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL HYDROCHLORIDE", "strength": "500 mg/20mL"}], "application_number": "ANDA214283", "marketing_category": "ANDA", "marketing_start_date": "20230308", "listing_expiration_date": "20261231"}