Prednisolone Acetate PF
Approved
Approval ID
6bb6cbee-6651-7e5a-e053-2991aa0a66dd
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 8, 2018
Manufacturers
FDA
ImprimisRx NJ
DUNS: 931390178
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Prednisolone Acetate PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-501
Product Classification
G
Generic Name
Prednisolone Acetate PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (1)
PREDNISOLONE ACETATEActive
Quantity: 10 mg in 1 mL
Code: 8B2807733D
Classification: ACTIB