PREDNISOLONE ACETATE PF- prednisolone acetate pf suspension/ 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 at 20° to 25° C (68° to 77° F)

Bottle Label

Bottle Label

PREDNISOLONE ACETATE PF 
prednisolone acetate pf suspension/ drops
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70261-501
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PREDNISOLONE ACETATE (UNII: 8B2807733D) (PREDNISOLONE - UNII:9PHQ9Y1OLM) PREDNISOLONE ACETATE10 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70261-501-055 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)

Revised: 5/2018
Document Id: 6bb6cbee-6652-7e5a-e053-2991aa0a66dd
Set id: 6bb6cbee-6651-7e5a-e053-2991aa0a66dd
Version: 1
Effective Time: 20180508
 
ImprimisRx NJ