mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
a-s medication solutions
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
mycophenolate mofetil 500 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500904275
Hyphenated Format
50090-4275
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
ANDA091249 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 180 TABLET, FILM COATED in 1 BOTTLE (50090-4275-0)
Packages (1)
Ingredients (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"}