mycophenolate mofetil

Generic: mycophenolate mofetil

Labeler: vistapharm, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mycophenolate mofetil
Generic Name mycophenolate mofetil
Labeler vistapharm, llc
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

mycophenolate mofetil 200 mg/mL

Manufacturer
VistaPharm, LLC

Identifiers & Regulatory

Product NDC 66689-307
Product ID 66689-307_1b2ac486-8e83-4fcf-998f-8e4f828cc406
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210370
Listing Expiration 2026-12-31
Marketing Start 2019-02-15

Pharmacologic Class

Classes
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66689307
Hyphenated Format 66689-307

Supplemental Identifiers

RxCUI
311880
UNII
9242ECW6R0

Packaging Origin

Original Packager
true

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 ANDA210370 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

mycophenolate mofetil (200 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b2ac486-8e83-4fcf-998f-8e4f828cc406", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["175d8b87-e06a-4c9e-b3de-378114b52274"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08)  / 250 mL in 1 BOTTLE, PLASTIC", "package_ndc": "66689-307-08", "marketing_start_date": "20190215"}], "brand_name": "Mycophenolate Mofetil", "product_id": "66689-307_1b2ac486-8e83-4fcf-998f-8e4f828cc406", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "66689-307", "generic_name": "Mycophenolate Mofetil", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA210370", "marketing_category": "ANDA", "marketing_start_date": "20190215", "listing_expiration_date": "20261231"}