Package 0093-7334-05

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 0093-7334-05
Digits Only 0093733405
Product NDC 0093-7334
Description

500 CAPSULE in 1 BOTTLE (0093-7334-05)

Marketing

Marketing Status
Marketed Since 2009-05-06
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": "d924ecfe-fba4-41ad-a1c1-e8ee06d76e67", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058"], "spl_set_id": ["b414303f-e6f3-4e22-a537-96be352b59a4"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-7334-01)", "package_ndc": "0093-7334-01", "marketing_start_date": "20090506"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0093-7334-05)", "package_ndc": "0093-7334-05", "marketing_start_date": "20090506"}], "brand_name": "Mycophenolate Mofetil", "product_id": "0093-7334_d924ecfe-fba4-41ad-a1c1-e8ee06d76e67", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0093-7334", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "250 mg/1"}], "application_number": "ANDA065491", "marketing_category": "ANDA", "marketing_start_date": "20090506", "listing_expiration_date": "20261231"}