Florexa
Florexa
Approved
Approval ID
d0842c09-4f4f-5209-e053-2a95a90a54d6
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.
Eflornithine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code82160-125
Product Classification
G
Generic Name
Eflornithine Hydrochloride
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 26, 2023
FDA Product Classification
INGREDIENTS (1)
EFLORNITHINE HYDROCHLORIDEActive
Quantity: 4170 mg in 30 g
Code: 4NH22NDW9H
Classification: ACTIR