PREDNISOLONE ACETATE PF suspension/ drops

Prednisolone Acetate PF by

Drug Labeling and Warnings

Prednisolone Acetate PF by is a Prescription medication manufactured, distributed, or labeled by ImprimisRx NJ. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STORAGE AND HANDLING

Store at 20° to 25° C (68° to 77° F)

Bottle Label

INGREDIENTS AND APPEARANCE

PREDNISOLONE ACETATE PF 
prednisolone acetate pf suspension/ drops

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 70261-501
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PREDNISOLONE ACETATE (UNII: 8B2807733D) (PREDNISOLONE - UNII:9PHQ9Y1OLM)	PREDNISOLONE ACETATE	10 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70261-501-05	5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	01/01/2018

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)