MOXIFLOXACIN PF- moxifloxacin pf injection, solution 
Imprimis NJOF, LLC

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.

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

Vial Label

Vial Label

MOXIFLOXACIN PF 
moxifloxacin pf injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:71384-511
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN5 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71384-511-0120 in 1 BOX01/05/2018
11 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/05/2018
Labeler - Imprimis NJOF, LLC (080431967)
Registrant - Imprimis NJOF, LLC (080431967)
Establishment
NameAddressID/FEIBusiness Operations
Imprimis NJOF, LLC080431967manufacture(71384-511)

Revised: 3/2020
Document Id: 9ff955f8-d64b-7991-e053-2995a90a8811
Set id: 9ff95904-783d-2929-e053-2995a90a49ec
Version: 11
Effective Time: 20200303
 
Imprimis NJOF, LLC