| 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 |