Hemmorex-HC
Hemmorex-HC
Approved
Approval ID
d625764a-6171-4802-9bc0-95e5785b8b7d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 5, 2021
Manufacturers
FDA
Laser Pharmaceuticals, LLC
DUNS: 614417132
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
hydrocortisone acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16477-202
Product Classification
G
Generic Name
hydrocortisone acetate
Product Specifications
Route of AdministrationRECTAL
Effective DateAugust 5, 2021
FDA Product Classification
INGREDIENTS (2)
HYDROCORTISONE ACETATEActive
Quantity: 30 mg in 1 1
Code: 3X7931PO74
Classification: ACTIB
HYDROGENATED PALM KERNEL OILInactive
Code: FM8D1RE2VP
Classification: IACT