TechneLite is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Lantheus Medical Imaging, Inc.. The primary component is Technetium Tc-99m Sodium Pertechnetate.
Product ID | 11994-090_769b2a90-555a-4674-accb-0c0a1cfa906c |
NDC | 11994-090 |
Product Type | Human Prescription Drug |
Proprietary Name | TechneLite |
Generic Name | Technetium Tc99m Generator |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA / NDA |
Application Number | NDA017771 |
Labeler Name | Lantheus Medical Imaging, Inc. |
Substance Name | TECHNETIUM TC-99M SODIUM PERTECHNETATE |
Active Ingredient Strength | 250 mCi/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1975-11-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Marketing Category | NDA |
Application Number | NDA017771 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1975-11-01 |
Ingredient | Strength |
---|---|
TECHNETIUM TC-99M SODIUM PERTECHNETATE | 250 mCi/mL |
SPL SET ID: | 3ae14c6b-3daf-4dd1-bbdb-e990fe8100e4 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
11994-090 | TechneLite | Technetium Tc99m Generator |
11994-091 | TechneLite | Technetium Tc99m Generator |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TECHNELITE 74254668 1812837 Live/Registered |
LANTHEUS MEDICAL IMAGING, INC. 1992-03-12 |
TECHNELITE 74254537 1812836 Live/Registered |
LANTHEUS MEDICAL IMAGING, INC. 1992-03-12 |