Package 50090-4275-0

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 50090-4275-0
Digits Only 5009042750
Product NDC 50090-4275
Product ID 50090-4275_bb6d7460-3900-4940-8564-af7078969144
Description

180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)

Marketing

Marketing Status
Marketed Since 2019-04-19
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bb6d7460-3900-4940-8564-af7078969144", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["b4170ad9-67f0-42ea-b694-6b80824a607a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)", "package_ndc": "50090-4275-0", "marketing_start_date": "20190419"}], "brand_name": "Mycophenolate Mofetil", "product_id": "50090-4275_bb6d7460-3900-4940-8564-af7078969144", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "50090-4275", "generic_name": "Mycophenolate Mofetil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA091249", "marketing_category": "ANDA", "marketing_start_date": "20111128", "listing_expiration_date": "20261231"}