Package 24338-018-01

Brand: myhibbin

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 24338-018-01
Digits Only 2433801801
Product NDC 24338-018
Description

1 BOTTLE, PLASTIC in 1 CARTON (24338-018-01) / 175 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2024-06-10
Brand myhibbin
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ab7e336c-d98f-495b-ad58-fc29eddd0c29", "openfda": {"upc": ["0324338018019"], "unii": ["9242ECW6R0"], "rxcui": ["311880", "2684851"], "spl_set_id": ["d9af72d6-7b3e-4c08-94b9-1d8b499cb7f9"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (24338-018-01)  / 175 mL in 1 BOTTLE, PLASTIC", "package_ndc": "24338-018-01", "marketing_start_date": "20240610"}], "brand_name": "MYHIBBIN", "product_id": "24338-018_ab7e336c-d98f-495b-ad58-fc29eddd0c29", "dosage_form": "SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "24338-018", "generic_name": "MYCOPHENOLATE MOFETIL", "labeler_name": "Azurity Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MYHIBBIN", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "NDA216482", "marketing_category": "NDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}