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
CAPSULE
Routes
Active Ingredients
mycophenolate mofetil 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4036
Product ID
70518-4036_3f9fc1fe-87b8-a8cf-e063-6394a90a2c38
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210181
Listing Expiration
2026-12-31
Marketing Start
2024-03-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184036
Hyphenated Format
70518-4036
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
ANDA210181 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 POUCH in 1 BOX (70518-4036-0) / 1 CAPSULE in 1 POUCH (70518-4036-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f9fc1fe-87b8-a8cf-e063-6394a90a2c38", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058"], "spl_set_id": ["d203775c-bf36-460c-bacf-3ab2348a514f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4036-0) / 1 CAPSULE in 1 POUCH (70518-4036-1)", "package_ndc": "70518-4036-0", "marketing_start_date": "20240311"}], "brand_name": "MYCOPHENOLATE MOFETIL", "product_id": "70518-4036_3f9fc1fe-87b8-a8cf-e063-6394a90a2c38", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "70518-4036", "generic_name": "MYCOPHENOLATE MOFETIL", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MYCOPHENOLATE MOFETIL", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "250 mg/1"}], "application_number": "ANDA210181", "marketing_category": "ANDA", "marketing_start_date": "20240311", "listing_expiration_date": "20261231"}