LATANOPROST PF- latanoprost pf solution/ drops 
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.

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Store under refrigeration 2° to 8° C (36° to 46° F)

Bottle Label

Bottle Label

LATANOPROST PF 
latanoprost pf solution/ drops
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70261-515
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LATANOPROST (UNII: 6Z5B6HVF6O) (LATANOPROST - UNII:6Z5B6HVF6O) LATANOPROST0.05 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70261-515-077.5 mL in 1 BOTTLE, DROPPER; 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)
Registrant - ImprimisRx NJ (931390178)
Establishment
NameAddressID/FEIBusiness Operations
Imprimis Pharmaceuticals080431967manufacture(70261-515)

Revised: 5/2018
Document Id: 6bb6aa59-65cb-2852-e053-2991aa0a087c
Set id: 6bb6aa59-65ca-2852-e053-2991aa0a087c
Version: 1
Effective Time: 20180508
 
ImprimisRx NJ