Package 0781-5175-10

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 0781-5175-10
Digits Only 0781517510
Product NDC 0781-5175
Description

1000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)

Marketing

Marketing Status
Marketed Since 2008-10-15
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": "8d255117-cfa8-4893-8e2e-945eee7b12c4", "openfda": {"upc": ["0307812067017"], "unii": ["9242ECW6R0"], "rxcui": ["199058", "200060"], "spl_set_id": ["99b2eb58-8d14-48fc-bbe1-aacb711a783e"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-5175-01)", "package_ndc": "0781-5175-01", "marketing_start_date": "20081015"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0781-5175-05)", "package_ndc": "0781-5175-05", "marketing_start_date": "20081015"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)", "package_ndc": "0781-5175-10", "marketing_start_date": "20081015"}], "brand_name": "Mycophenolate Mofetil", "product_id": "0781-5175_8d255117-cfa8-4893-8e2e-945eee7b12c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0781-5175", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA065451", "marketing_category": "ANDA", "marketing_start_date": "20081015", "listing_expiration_date": "20261231"}