Package 31722-879-05

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 31722-879-05
Digits Only 3172287905
Product NDC 31722-879
Description

500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05)

Marketing

Marketing Status
Marketed Since 2024-10-22
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": "48432e06-b34c-4277-e063-6394a90a6ba0", "openfda": {"upc": ["0331722879019"], "unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["c3ded171-89da-4644-9ee8-dbcf6258036f"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-879-01)", "package_ndc": "31722-879-01", "marketing_start_date": "20241022"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05)", "package_ndc": "31722-879-05", "marketing_start_date": "20241022"}], "brand_name": "Mycophenolate Mofetil", "product_id": "31722-879_48432e06-b34c-4277-e063-6394a90a6ba0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "31722-879", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA208119", "marketing_category": "ANDA", "marketing_start_date": "20241022", "listing_expiration_date": "20271231"}