Mycophenolate Mofetil

Generic: mycophenolate mofetil

Labeler: Mylan Institutional Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Mycophenolate Mofetil
Generic Name mycophenolate mofetil
Labeler Mylan Institutional Inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

MYCOPHENOLATE MOFETIL 500 mg/1

Identifiers & Regulatory

Product NDC 51079-379
Product ID 51079-379_312ec7cc-9e59-56a3-e063-6394a90a828f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065521
Marketing Start 2009-06-01
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079379
Hyphenated Format 51079-379

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 ANDA065521 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-379-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-379-01)
source: ndc

Packages (1)

Ingredients (1)

MYCOPHENOLATE MOFETIL (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "312ec7cc-9e59-56a3-e063-6394a90a828f", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["199058", "200060"], "spl_set_id": ["52907069-4a29-4351-a830-a9ee86b5ff7c"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-379-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-379-01)", "package_ndc": "51079-379-20", "marketing_end_date": "20260228", "marketing_start_date": "20090601"}], "brand_name": "Mycophenolate Mofetil", "product_id": "51079-379_312ec7cc-9e59-56a3-e063-6394a90a828f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "51079-379", "generic_name": "mycophenolate mofetil", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA065521", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20090601"}