MOXIFLOXACIN PF injection, solution

Moxifloxacin PF by

Drug Labeling and Warnings

Moxifloxacin PF by is a Prescription medication manufactured, distributed, or labeled by ImprimisRx NJ, Imprimis Pharmaceuticals. 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

MOXIFLOXACIN PF 
moxifloxacin pf injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 70261-511
Route of Administration	INTRAOCULAR

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

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	8 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70261-511-01	1 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	01/01/2018

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

Labeler - ImprimisRx NJ (931390178)

Registrant - ImprimisRx NJ (931390178)

Establishment
Name	Address	ID/FEI	Business Operations
Imprimis Pharmaceuticals		080431967	manufacture(70261-511)