Package 70518-4377-0
Brand: mycophenolate mofetil
Generic: mycophenolate mofetilPackage Facts
Identity
Package NDC
70518-4377-0
Digits Only
7051843770
Product NDC
70518-4377
Description
100 POUCH in 1 BOX (70518-4377-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4377-1)
Marketing
Marketing Status
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": "38dd4fa9-8b2d-47b6-e063-6294a90a1b7b", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["84c6f6bb-8924-4da5-9629-126197195f83"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4377-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4377-1)", "package_ndc": "70518-4377-0", "marketing_start_date": "20250630"}], "brand_name": "Mycophenolate mofetil", "product_id": "70518-4377_38dd4fa9-8b2d-47b6-e063-6294a90a1b7b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70518-4377", "generic_name": "Mycophenolate mofetil", "labeler_name": "REMEDYREPACK INC.", "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": "20250630", "listing_expiration_date": "20261231"}