myhibbin
Generic: mycophenolate mofetil
Labeler: azurity pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
myhibbin
Generic Name
mycophenolate mofetil
Labeler
azurity pharmaceuticals, inc.
Dosage Form
SUSPENSION
Routes
Active Ingredients
mycophenolate mofetil 200 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24338018
Hyphenated Format
24338-018
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
myhibbin (source: ndc)
Generic Name
mycophenolate mofetil (source: ndc)
Application Number
NDA216482 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (24338-018-01) / 175 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": "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"}