Package 63629-9582-1

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 63629-9582-1
Digits Only 6362995821
Product NDC 63629-9582
Description

120 TABLET in 1 BOTTLE (63629-9582-1)

Marketing

Marketing Status
Marketed Since 2022-11-15
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "66ccb233-553a-4ada-afb7-4f51a6f72214", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["0f1704e2-a66a-4be5-8127-ebb5947c7b64"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-9582-1)", "package_ndc": "63629-9582-1", "marketing_start_date": "20221115"}], "brand_name": "mycophenolate mofetil", "product_id": "63629-9582_66ccb233-553a-4ada-afb7-4f51a6f72214", "dosage_form": "TABLET", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "63629-9582", "generic_name": "mycophenolate mofetil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA065416", "marketing_category": "ANDA", "marketing_start_date": "20090504", "listing_expiration_date": "20261231"}