DEX-MOXI- dexamethasone phosphate - moxifloxacin injection, solution

Dex-Moxi by

Drug Labeling and Warnings

Dex-Moxi by is a Prescription medication manufactured, distributed, or labeled by Imprimis NJOF, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STORAGE AND HANDLING

Store at 20° to 25° C (68° to 77° F)

Vial Label

INGREDIENTS AND APPEARANCE

DEX-MOXI 
dexamethasone phosphate - moxifloxacin injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71384-512
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P) (DEXAMETHASONE - UNII:7S5I7G3JQL)	DEXAMETHASONE PHOSPHATE	1 mg  in 1 mL
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P)	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71384-512-01	20 in 1 BOX	01/05/2018
1		1 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/05/2018

Labeler - Imprimis NJOF, LLC (080431967)

Registrant - Imprimis NJOF, LLC (080431967)