Aquax-H
Aquax-H
Approved
Approval ID
d042d188-4afc-af1d-e053-2a95a90a386c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 26, 2023
Manufacturers
FDA
Pella Pharmaceuticals Co. ltd
DUNS: 562370925
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Hydrocortisone Butyrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code82160-127
Product Classification
G
Generic Name
Hydrocortisone Butyrate
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 26, 2023
FDA Product Classification
INGREDIENTS (1)
HYDROCORTISONE BUTYRATEActive
Quantity: 30 mg in 30 g
Code: 05RMF7YPWN
Classification: ACTIB