Package 0904-7078-61

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 0904-7078-61
Digits Only 0904707861
Product NDC 0904-7078
Description

100 BLISTER PACK in 1 CAPSULE (0904-7078-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2010-11-06
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": "f2afb582-0575-44fd-95f9-9a019638ea6c", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["d176199c-dc3f-48c8-b7d2-c5d0a6a242fe"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CAPSULE (0904-7078-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7078-61", "marketing_start_date": "20101106"}], "brand_name": "Mycophenolate mofetil", "product_id": "0904-7078_f2afb582-0575-44fd-95f9-9a019638ea6c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0904-7078", "generic_name": "Mycophenolate mofetil", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA090456", "marketing_category": "ANDA", "marketing_start_date": "20101106", "listing_expiration_date": "20261231"}