Moxifloxacin PF
Approved
Approval ID
9ff95904-783d-2929-e053-2995a90a49ec
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 3, 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.
Moxifloxacin PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71384-511
Product Classification
G
Generic Name
Moxifloxacin PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMarch 3, 2020
FDA Product Classification
INGREDIENTS (1)
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATEActive
Quantity: 5 mg in 1 mL
Code: B8956S8609
Classification: ACTIM