myhibbin

Generic: mycophenolate mofetil

Labeler: azurity pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name myhibbin
Generic Name mycophenolate mofetil
Labeler azurity pharmaceuticals, inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

mycophenolate mofetil 200 mg/mL

Manufacturer
Azurity Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 24338-018
Product ID 24338-018_ab7e336c-d98f-495b-ad58-fc29eddd0c29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA216482
Listing Expiration 2026-12-31
Marketing Start 2024-06-10

Pharmacologic Class

Classes
antimetabolite immunosuppressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24338018
Hyphenated Format 24338-018

Supplemental Identifiers

RxCUI
311880 2684851
UPC
0324338018019
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 myhibbin (source: ndc)
Generic Name mycophenolate mofetil (source: ndc)
Application Number NDA216482 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (24338-018-01) / 175 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": "ab7e336c-d98f-495b-ad58-fc29eddd0c29", "openfda": {"upc": ["0324338018019"], "unii": ["9242ECW6R0"], "rxcui": ["311880", "2684851"], "spl_set_id": ["d9af72d6-7b3e-4c08-94b9-1d8b499cb7f9"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (24338-018-01)  / 175 mL in 1 BOTTLE, PLASTIC", "package_ndc": "24338-018-01", "marketing_start_date": "20240610"}], "brand_name": "MYHIBBIN", "product_id": "24338-018_ab7e336c-d98f-495b-ad58-fc29eddd0c29", "dosage_form": "SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "24338-018", "generic_name": "MYCOPHENOLATE MOFETIL", "labeler_name": "Azurity Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MYHIBBIN", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "NDA216482", "marketing_category": "NDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}