Sodium FluorideF 18
- Product NDC
- 76167-002
- 11-digit product format
- 761670002
- Labeler code
- 76167
- Product ID
- 76167-002_c849e41b-ab04-4c4b-a055-57e87ce42915
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE F-18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Children's Hospital of Michigan
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-12
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE F-18
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76167-002-30 | Sodium FluorideF 18F 18 | 30 mL in 1 VIAL, MULTI-DOSE | INJECTION | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76167-002 | SODIUM FLUORIDEF 18 F 18 (SODIUM FLUORIDE F-18) INJECTION [CHILDREN'S HOSPITAL OF MICHIGAN] | 1 | Legacy NDC, 1 package rows | 20120612_25418092-48c3-4ac0-92b0-72a6289d423f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 76167-002-30 | 76167000230 | 30 mL in 1 VIAL, MULTI-DOSE | 30 ml | Historical |