Dex-Moxi PF
Approved
Approval ID
6bb78fd2-5d72-1b41-e053-2991aa0af497
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.
Dexamethasone - Moxifloxacin PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-512
Product Classification
G
Generic Name
Dexamethasone - Moxifloxacin PF
Product Specifications
Route of AdministrationINTRAOCULAR
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (2)
DEXAMETHASONE SODIUM PHOSPHATEActive
Quantity: 1 mg in 1 mL
Code: AI9376Y64P
Classification: ACTIR
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATEActive
Quantity: 5 mg in 1 mL
Code: B8956S8609
Classification: ACTIM