Product NDC: | 65909-089 |
Proprietary Name: | STRONTIUM CHLORIDE Sr-89 |
Non Proprietary Name: | STRONTIUM CHLORIDE SR-89 |
Active Ingredient(s): | 1 mCi/mL & nbsp; STRONTIUM CHLORIDE SR-89 |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65909-089 |
Labeler Name: | BIO NUCLEONICS INC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075941 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030106 |
Package NDC: | 65909-089-01 |
Package Description: | 5 mL in 1 VIAL (65909-089-01) |
NDC Code | 65909-089-01 |
Proprietary Name | STRONTIUM CHLORIDE Sr-89 |
Package Description | 5 mL in 1 VIAL (65909-089-01) |
Product NDC | 65909-089 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | STRONTIUM CHLORIDE SR-89 |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20030106 |
Marketing Category Name | ANDA |
Labeler Name | BIO NUCLEONICS INC |
Substance Name | STRONTIUM CHLORIDE SR-89 |
Strength Number | 1 |
Strength Unit | mCi/mL |
Pharmaceutical Classes |