Drug Labeling and Warnings

Drug Details

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DEX-MOXI- dexamethasone phosphate - moxifloxacin 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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Store at 20° to 25° C (68° to 77° F)

Vial Label

Vial Label

DEX-MOXI 
dexamethasone phosphate - moxifloxacin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 71384-512
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P) (DEXAMETHASONE - UNII:7S5I7G3JQL) DEXAMETHASONE PHOSPHATE1 mg  in 1 mL
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (UNII: B8956S8609) (MOXIFLOXACIN - UNII:U188XYD42P) MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE5 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71384-512-0120 in 1 BOX01/05/2018
11 mL in 1 VIAL, SINGLE-USE; 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(71384-512)

Revised: 1/2018
 
Imprimis NJOF, LLC


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