MOXIFLOXACIN PF injection, solution

Moxifloxacin PF by

Drug Labeling and Warnings

Moxifloxacin PF 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

20 0 to 25 0 C (*68 0 to 77 0 F)

Vial Label

INGREDIENTS AND APPEARANCE

MOXIFLOXACIN PF 
moxifloxacin pf injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71384-511
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P)	MOXIFLOXACIN	5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71384-511-01	20 in 1 BOX	01/05/2018
1		1 mL in 1 VIAL, SINGLE-DOSE; 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)

Establishment
Name	Address	ID/FEI	Business Operations
Imprimis NJOF, LLC		080431967	manufacture(71384-511)