Package 59651-646-26

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 59651-646-26
Digits Only 5965164626
Product NDC 59651-646
Product ID 59651-646_83531645-459d-4746-bc46-2d32928e9417
Description

1 BOTTLE in 1 CARTON (59651-646-26) / 225 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-09-26
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": ["ORAL"], "spl_id": "83531645-459d-4746-bc46-2d32928e9417", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["20fa7709-a203-481f-aaf4-e98fab1acd0d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59651-646-26)  / 225 mL in 1 BOTTLE", "package_ndc": "59651-646-26", "marketing_start_date": "20240926"}], "brand_name": "MYCOPHENOLATE MOFETIL", "product_id": "59651-646_83531645-459d-4746-bc46-2d32928e9417", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "59651-646", "generic_name": "mycophenolate mofetil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MYCOPHENOLATE MOFETIL", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA218227", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}