mycophenolate mofetil

Generic: mycophenolate mofetil

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

Drug Facts

Product Profile

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

mycophenolate mofetil 200 mg/mL

Manufacturer
Ascend Laboratories, LLC

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
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877230
Hyphenated Format 67877-230

Supplemental Identifiers

RxCUI
311880
UPC
0367877230221
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 ANDA203005 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) / 225 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": "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"}