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Medicine

Fludeoxyglucose f-18 200 mCi/mL injection

Fludeoxyglucose f-18 · Intravenous
Available on requestPrescription onlyUS FDAGeneric name

Fludeoxyglucose f-18 200 mCi/mL injection is a generic prescription medicine for intravenous use, made by 2 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store the Fludeoxyglucose F 18 Injection vial upright in a lead shielded…

Key facts

Active ingredient (INN)
Fludeoxyglucose f-18
Brand
Sold under the generic name
Strength
200 mCi/mL
Dosage form
Injection
Route
Intravenous
Packs
1 vial, 25 mL
Manufacturers
PETNET SolutionsTrustees of the University of Pennsylvania
Origin register
US FDA, United States
Storage
Store the Fludeoxyglucose F 18 Injection vial upright in a lead shielded container at 25°C (77°F), excursions permitted to 15-30°C (59-86°F). Store and dispose of Fludeoxyglucose F 18 Injection in accordance with the regulations and a general license, or its equivalent, of an Agreement State or a Licensing State.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
V09IX04 Fludeoxyglucose f-18
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
29 July 2008
Identifiers
DailyMed set ID caaa9ab5-e3f4-489d-9f4c-0ecbee6fca83, 84f1aeab-685d-47fd-a8e9-e724979c4ce6NDC 40028-511, 40098-101Application ANDA079086, ANDA203801

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
1 vial, multi-dose in 1 can / 50 mL in 1 vial, multi-dose40028-511-50PETNET Solutions29 July 2008
1 vial, multi-dose in 1 can / 100 mL in 1 vial, multi-dose40028-511-99PETNET Solutions29 July 2008
25 mL in 1 vial, multi-dose40098-101-19Trustees of the University of Pennsylvania30 October 2014

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 19 August 1994Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Other strengths and forms of Fludeoxyglucose f-18

Clinical summary

Fludeoxyglucose f-18 is a radioactive diagnostic agent indicated for positron emission tomography (PET) imaging in settings, among other approved uses. It is available as injection for intravenous use. MedsAcross supplies Fludeoxyglucose f-18 for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Fludeoxyglucose f-18

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Fludeoxyglucose f-18 200 mCi/mL injection for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.