mycophenolate mofetil

Generic: mycophenolate mofetil

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mycophenolate mofetil
Generic Name mycophenolate mofetil
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mycophenolate mofetil 500 mg/1

Manufacturer
American Health Packaging

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
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687438
Hyphenated Format 60687-438

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 ANDA090456 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)
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": "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"}