mycophenolate mofetil

Generic: mycophenolate mofetil

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mycophenolate mofetil
Generic Name mycophenolate mofetil
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mycophenolate mofetil 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4275
Product ID 50090-4275_bb6d7460-3900-4940-8564-af7078969144
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091249
Listing Expiration 2026-12-31
Marketing Start 2011-11-28

Pharmacologic Class

Classes
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904275
Hyphenated Format 50090-4275

Supplemental Identifiers

RxCUI
200060
UNII
9242ECW6R0

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 ANDA091249 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)
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": "bb6d7460-3900-4940-8564-af7078969144", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["b4170ad9-67f0-42ea-b694-6b80824a607a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)", "package_ndc": "50090-4275-0", "marketing_start_date": "20190419"}], "brand_name": "Mycophenolate Mofetil", "product_id": "50090-4275_bb6d7460-3900-4940-8564-af7078969144", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "50090-4275", "generic_name": "Mycophenolate Mofetil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA091249", "marketing_category": "ANDA", "marketing_start_date": "20111128", "listing_expiration_date": "20261231"}