TechneLite

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 (canonical bytes are SHA-256 checked before publication)

Brand name: TechneLite
Generic name: TECHNETIUM TC99M GENERATOR
Manufacturer: Lantheus Medical Imaging, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 3ae14c6b-3daf-4dd1-bbdb-e990fe8100e4
SPL ID: ffbbca75-06da-47fc-bc12-ceefdf308162
Version: 17
Effective date: 2024-11-01
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:41:59

Harmonized routes table
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.

Harmonized identifiers page 1 of 2 · 66 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	017771	derived:openfda.application_number
application number		NDA017771	openfda.application_number
brand name		TechneLite	openfda.brand_name
generic name		TECHNETIUM TC99M GENERATOR	openfda.generic_name
manufacturer name		Lantheus Medical Imaging, Inc.	openfda.manufacturer_name
ndc	package	11994-091-13	openfda.package_ndc
ndc	package	11994-090-01	openfda.package_ndc
ndc	package	11994-091-11	openfda.package_ndc
ndc	package	11994-090-92	openfda.package_ndc
ndc	package	11994-091-04	openfda.package_ndc
ndc	package	11994-091-05	openfda.package_ndc
ndc	package	11994-090-73	openfda.package_ndc
ndc	package	11994-091-73	openfda.package_ndc
ndc	package	11994-091-01	openfda.package_ndc
ndc	package	11994-091-06	openfda.package_ndc
ndc	package	11994-091-10	openfda.package_ndc
ndc	package	11994-090-36	openfda.package_ndc
ndc	package	11994-091-03	openfda.package_ndc
ndc	package	11994-090-03	openfda.package_ndc
ndc	package	11994-091-36	openfda.package_ndc
ndc	package	11994-091-92	openfda.package_ndc
ndc	package	11994-090-09	openfda.package_ndc
ndc	package	11994-091-12	openfda.package_ndc
ndc	package	11994-090-12	openfda.package_ndc
ndc	package	11994-090-11	openfda.package_ndc
ndc	package	11994-090-06	openfda.package_ndc
ndc	package	11994-090-04	openfda.package_ndc
ndc	package	11994-090-05	openfda.package_ndc
ndc	package	11994-090-10	openfda.package_ndc
ndc	package	11994-091-07	openfda.package_ndc
ndc	package	11994-091-09	openfda.package_ndc
ndc	package	11994-090-13	openfda.package_ndc
ndc	package	11994-090-07	openfda.package_ndc
ndc	product	11994-091	openfda.product_ndc
ndc	product	11994-090	openfda.product_ndc
ndc11	package	11994009173	derived:openfda.package_ndc
ndc11	package	11994009013	derived:openfda.package_ndc
ndc11	package	11994009111	derived:openfda.package_ndc
ndc11	package	11994009101	derived:openfda.package_ndc
ndc11	package	11994009105	derived:openfda.package_ndc

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Radiation risks associated with the use of Sodium Pertechnetate Tc 99m Injection are greater in children than in adults and, in general, the younger the child, the greater the risk owing to greater absorbed radiation doses and longer life-expectancy. These greater risks should be taken firmly into account in all benefit-risk assessments involving children. Long-term cumulative radiation exposure may be associated with an increased risk of cancer.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS: Allergic reactions including anaphylaxis have been reported infrequently following the administration of Sodium Pertechnetate Tc 99m Injection.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.