mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
mycophenolate mofetil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2767
Product ID
70518-2767_3e501eaf-87d3-7e12-e063-6294a90a8353
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090456
Listing Expiration
2026-12-31
Marketing Start
2020-06-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182767
Hyphenated Format
70518-2767
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
mycophenolate mofetil (source: ndc)
Generic Name
mycophenolate mofetil (source: ndc)
Application Number
ANDA090456 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 POUCH in 1 BOX (70518-2767-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2767-2)
Packages (1)
Ingredients (1)
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"}