Prednisolone (Page 3 of 3)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ML LABEL
(click image for full-size original)

PREDNISOLONE
prednisolone solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:67296-1656(NDC:50383-042)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISOLONE (PREDNISOLONE) PREDNISOLONE 15 mg in 5 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
ANHYDROUS CITRIC ACID
BENZOIC ACID
CHERRY
EDETATE DISODIUM
FD&C BLUE NO. 1
FD&C RED NO. 40
GLYCERIN
PROPYLENE GLYCOL
SACCHARIN SODIUM
SUCROSE
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:67296-1656-6 60 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040401 02/27/2003
Labeler — RedPharm Drug, Inc. (828374897)
Establishment
Name Address ID/FEI Operations
EPM Packaging, Inc. 079124340 repack (67296-1656)

Revised: 01/2022 RedPharm Drug, Inc.

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