TechneLite

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

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
2026-08-01
Applications, Product NDCs, Package NDCs table
ApplicationsProduct NDCsPackage NDCsRxCUIsUNIIsRoutes
NDA01777111994-090, 11994-09111994-090-36, 11994-090-73, 11994-090-92, 11994-090-01, 11994-090-03, 11994-090-04, 11994-090-05, 11994-090-06, 11994-090-07, 11994-090-09, 11994-090-10, 11994-090-11, 11994-090-12, 11994-090-13, 11994-091-36, 11994-091-73, 11994-091-92, 11994-091-01, 11994-091-03, 11994-091-04, 11994-091-05, 11994-091-06, 11994-091-07, 11994-091-09, 11994-091-10, 11994-091-11, 11994-091-12, 11994-091-13A0730CX801INTRAVENOUS

Warnings cross-check#

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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#

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adverse reactions

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