TRIAMCINOLONE-MOXIFLOXACIN PF injection, suspension

Triamcinolone-Moxifloxacin PF by

Drug Labeling and Warnings

Triamcinolone-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

Store at 20° to 25° C (68° to 77° F)

Package Label

INGREDIENTS AND APPEARANCE

TRIAMCINOLONE-MOXIFLOXACIN PF 
triamcinolone-moxifloxacin pf injection, suspension

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71384-510
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA)	TRIAMCINOLONE ACETONIDE	15 mg  in 1 mL
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P)	MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	1 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71384-510-01	20 in 1 BOX	01/05/2018
1		0.6 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)