Glofil-125
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Glofil-125
- Generic name
- SODIUM IOTHALAMATE I-125 INJECTION
- Manufacturer
- Iso-Tex Diagnostics, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7f250086-2837-484b-9674-e09856b34cb0
- SPL ID
- 03a98b4c-213b-4537-8d3a-aaa9f9f1cc9b
- Version
- 4
- Effective date
- 2019-12-09
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:33:49
| Harmonized routes |
|---|
| INTRAVENOUS |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 017279 | derived:openfda.application_number |
| application number | NDA017279 | openfda.application_number | |
| brand name | Glofil-125 | openfda.brand_name | |
| generic name | SODIUM IOTHALAMATE I-125 INJECTION | openfda.generic_name | |
| manufacturer name | Iso-Tex Diagnostics, Inc. | openfda.manufacturer_name | |
| ndc | package | 50914-7729-2 | openfda.package_ndc |
| ndc | product | 50914-7729 | openfda.product_ndc |
| ndc11 | package | 50914772902 | derived:openfda.package_ndc |
| spl id | 03a98b4c-213b-4537-8d3a-aaa9f9f1cc9b | id | |
| spl set id | 7f250086-2837-484b-9674-e09856b34cb0 | set_id | |
| unii | 31J5U3Q9ZN | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS None known
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS None Reported
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.