Package 70518-2767-1

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 70518-2767-1
Digits Only 7051827671
Product NDC 70518-2767
Description

100 POUCH in 1 BOX (70518-2767-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2767-2)

Marketing

Marketing Status
Marketed Since 2021-12-16
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": "3e501eaf-87d3-7e12-e063-6294a90a8353", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["afb59492-2bb1-4cf1-af4b-a5020b56c124"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2767-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2767-2)", "package_ndc": "70518-2767-1", "marketing_start_date": "20211216"}], "brand_name": "Mycophenolate mofetil", "product_id": "70518-2767_3e501eaf-87d3-7e12-e063-6294a90a8353", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70518-2767", "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": "20200608", "listing_expiration_date": "20261231"}