MedPath

Hybrisil

Approved
Approval ID

f8432414-d8a6-4597-a226-61fd09a80e0c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 22, 2011

Manufacturers
FDA

BioZone Laboratories, Inc.

DUNS: 555564293

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Methylprednisolone Acetate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code55379-405
Product Classification
G
Generic Name
Methylprednisolone Acetate
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 22, 2011
FDA Product Classification

INGREDIENTS (1)

Methylprednisolone AcetateActive
Quantity: 10 mg in 1 g
Code: 43502P7F0P
Classification: ACTIB

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Hybrisil - FDA Drug Approval Details