TRIAMCINOLONE-MOXIFLOXACIN PF- triamcinolone-moxifloxacin pf suspension 
ImprimisRx NJ

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

Store at 20° to 25° C (68° to 77° F)

Vial Label

TRIAMCINOLONE-MOXIFLOXACIN PF 
triamcinolone-moxifloxacin pf suspension
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70261-510
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MOXIFLOXACIN HYDROCHLORIDE (UNII: C53598599T) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN1 mg  in 1 mL
TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE15 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70261-510-010.6 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product01/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/2018
Labeler - ImprimisRx NJ (931390178)

Revised: 2/2018
Document Id: 6636df26-31bb-6b09-e053-2991aa0a4c6f
Set id: 6636df26-31ba-6b09-e053-2991aa0a4c6f
Version: 1
Effective Time: 20180227
 
ImprimisRx NJ