mycophenolate mofetil

Generic: mycophenolate mofetil

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mycophenolate mofetil
Generic Name mycophenolate mofetil
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

mycophenolate mofetil 500 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3767
Product ID 68071-3767_2b9b049f-8ec4-0535-e063-6394a90afc7a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090456
Listing Expiration 2026-12-31
Marketing Start 2010-11-06

Pharmacologic Class

Classes
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713767
Hyphenated Format 68071-3767

Supplemental Identifiers

RxCUI
200060
UPC
0368071376760
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
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)
source: ndc

Packages (1)

68071-3767-6 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)

Ingredients (1)

mycophenolate mofetil (500 mg/1)

Linked Drug Pages (1)

Mycophenolate mofetil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b9b049f-8ec4-0535-e063-6394a90afc7a", "openfda": {"upc": ["0368071376760"], "unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["2b9ae8ff-f2bc-ccef-e063-6294a90a76da"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)", "package_ndc": "68071-3767-6", "marketing_start_date": "20250113"}], "brand_name": "Mycophenolate mofetil", "product_id": "68071-3767_2b9b049f-8ec4-0535-e063-6394a90afc7a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "68071-3767", "generic_name": "Mycophenolate mofetil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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": "20101106", "listing_expiration_date": "20261231"}