mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: vistapharm, llcDrug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
vistapharm, llc
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
mycophenolate mofetil 200 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66689307
Hyphenated Format
66689-307
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 200 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
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"}