mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
mycophenolate mofetil 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-438
Product ID
60687-438_45762f11-5cf6-b346-e063-6394a90a6199
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090456
Listing Expiration
2026-12-31
Marketing Start
2019-06-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687438
Hyphenated Format
60687-438
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 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45762f11-5cf6-b346-e063-6394a90a6199", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["8015f042-54fb-4a7a-a10b-6219e1a450c8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)", "package_ndc": "60687-438-01", "marketing_start_date": "20190614"}], "brand_name": "Mycophenolate mofetil", "product_id": "60687-438_45762f11-5cf6-b346-e063-6394a90a6199", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "60687-438", "generic_name": "Mycophenolate Mofetil", "labeler_name": "American Health Packaging", "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": "20190614", "listing_expiration_date": "20261231"}