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NDC 24562-0002-30 Sodium Fluoride F 18 200 mCi/mL Details
Sodium Fluoride F 18 200 mCi/mL
Sodium Fluoride F 18 is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Biomedical Research Foundation of Northwest Louisiana. The primary component is SODIUM FLUORIDE F-18.
Product Information
NDC | 24562-0002 |
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Product ID | 24562-002_0e9be92f-b0e1-4c34-a786-6a84fdfb9833 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Sodium Fluoride F 18 |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | SODIUM FLUORIDE F-18 |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 200 |
Active Ingredient Units | mCi/mL |
Substance Name | SODIUM FLUORIDE F-18 |
Labeler Name | Biomedical Research Foundation of Northwest Louisiana |
Pharmaceutical Class | Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA204351 |
Listing Certified Through | 2024-12-31 |
Package
NDC 24562-0002-30 (24562000230)
NDC Package Code | 24562-002-30 |
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Billing NDC | 24562000230 |
Package | 30 mL in 1 VIAL, MULTI-DOSE (24562-002-30) |
Marketing Start Date | 2015-01-22 |
NDC Exclude Flag | N |
Pricing Information | N/A |