Triamcinolone-Moxifloxacin PF
Approved
Approval ID
62fce8cd-0956-2830-e053-2991aa0a041c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 10, 2020
Manufacturers
FDA
Imprimis NJOF, LLC
DUNS: 080431967
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Triamcinolone-Moxifloxacin PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71384-510
Product Classification
G
Generic Name
Triamcinolone-Moxifloxacin PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateFebruary 10, 2020
FDA Product Classification
INGREDIENTS (2)
TRIAMCINOLONE ACETONIDEActive
Quantity: 15 mg in 1 mL
Code: F446C597KA
Classification: ACTIB
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATEActive
Quantity: 1 mg in 1 mL
Code: B8956S8609
Classification: ACTIB