FLUDEOXYGLUCOSE F 18 (Page 4 of 4)

17 PATIENT COUNSELING INFORMATION

Instruct patients in procedures that increase renal clearance of radioactivity. Encourage patients to:

  • drink water or other fluids (as tolerated) in the 4 hours before their PET study.
  • void as soon as the imaging study is completed and as often as possible thereafter for at least one hour.

Manufactured by:

UIHC — P E T Imaging Center

0911Z JPP

200 Hawkins Drive

Iowa City, IA

Distributed by:

UIHC — P E T Imaging Center

0911Z JPP

200 Hawkins Drive

Iowa City, IA

Label
(click image for full-size original)
FLUDEOXYGLUCOSE F 18
fludeoxyglucose f-18 injection
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:24417-001
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLUDEOXYGLUCOSE F-18 (FLUDEOXYGLUCOSE F-18) FLUDEOXYGLUCOSE F-18 300 mCi in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM CITRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24417-001-30 30 mL in 1 VIAL, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA203990 12/12/2011
Labeler — UIHC-P E T IMAGING CENTER (063513265)
Establishment
Name Address ID/FEI Operations
UIHC-P E T IMAGING CENTER 063513265 positron emission tomography drug production (24417-001)

Revised: 11/2019 UIHC-P E T IMAGING CENTER

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