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Sodium Fluoride
Sodium Fluoride - 16129-002-10 - (SODIUM FLUORIDE F 18)
Drug Information of Sodium Fluoride
| Product NDC: | 16129-002 |
| Proprietary Name: | Sodium Fluoride |
| Non Proprietary Name: | SODIUM FLUORIDE F 18 |
| Active Ingredient(s): | 200 mCi/mL & nbsp; SODIUM FLUORIDE F 18 |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Fluoride
| Product NDC: | 16129-002 |
| Labeler Name: | Shertech Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110323 |
Package Information of Sodium Fluoride
| Package NDC: | 16129-002-10 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (16129-002-10) |
NDC Information of Sodium Fluoride
| NDC Code | 16129-002-10 |
| Proprietary Name | Sodium Fluoride |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (16129-002-10) |
| Product NDC | 16129-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM FLUORIDE F 18 |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110323 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Shertech Laboratories, LLC |
| Substance Name | SODIUM FLUORIDE F-18 |
| Strength Number | 200 |
| Strength Unit | mCi/mL |
| Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |
