Latanoprost PF

LATANOPROST PF- latanoprost 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.

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

Bottle Label
(click image for full-size original)

LATANOPROST PF
latanoprost pf solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70261-515
Route of Administration OPHTHALMIC DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LATANOPROST (LATANOPROST) LATANOPROST 0.05 mg in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70261-515-07 7.5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/01/2018
Labeler — ImprimisRx NJ (931390178)
Registrant — ImprimisRx NJ (931390178)
Establishment
Name Address ID/FEI Operations
Imprimis Pharmaceuticals 080431967 manufacture (70261-515)

Revised: 05/2018 ImprimisRx NJ

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