mycophenolate mofetil
Generic: mycophenolate mofetil
Labeler: ascend laboratories, llcDrug Facts
Product Profile
Brand Name
mycophenolate mofetil
Generic Name
mycophenolate mofetil
Labeler
ascend laboratories, llc
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
mycophenolate mofetil 200 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67877-230
Product ID
67877-230_d57b5ef3-52b0-473c-aa54-3208566e5909
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203005
Listing Expiration
2026-12-31
Marketing Start
2014-11-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877230
Hyphenated Format
67877-230
Supplemental Identifiers
RxCUI
UPC
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
ANDA203005 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) / 225 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": "d57b5ef3-52b0-473c-aa54-3208566e5909", "openfda": {"upc": ["0367877230221"], "unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["21ff53b0-b4ba-4473-91e4-76ef41681064"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) / 225 mL in 1 BOTTLE, PLASTIC", "package_ndc": "67877-230-22", "marketing_start_date": "20141117"}], "brand_name": "Mycophenolate mofetil", "product_id": "67877-230_d57b5ef3-52b0-473c-aa54-3208566e5909", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "67877-230", "generic_name": "Mycophenolate mofetil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA203005", "marketing_category": "ANDA", "marketing_start_date": "20141117", "listing_expiration_date": "20261231"}