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NDC 17156-0022-05 CERETEC 0.5 mg/5mL Details
CERETEC 0.5 mg/5mL
CERETEC is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Medi-Physics Inc. dba GE Healthcare.. The primary component is TECHNETIUM TC-99M EXAMETAZIME.
Product Information
| NDC | 17156-0022 |
|---|---|
| Product ID | 17156-022_87cca989-b750-4ca7-9b5a-6f00d0457c46 |
| Associated GPIs | |
| GCN Sequence Number | 077678 |
| GCN Sequence Number Description | kit prep Tc-99m/exametazime VIAL 0.5 MG INTRAVEN |
| HIC3 | D0V |
| HIC3 Description | GASTROINTESTINAL RADIOACTIVE DIAGNOSTICS |
| GCN | 43775 |
| HICL Sequence Number | 024613 |
| HICL Sequence Number Description | KIT FOR PREP TC-99M/EXAMETAZIME |
| Brand/Generic | Brand |
| Proprietary Name | CERETEC |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | TECHNETIUM TC-99M EXAMETAZIME |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 0.5 |
| Active Ingredient Units | mg/5mL |
| Substance Name | TECHNETIUM TC-99M EXAMETAZIME |
| Labeler Name | Medi-Physics Inc. dba GE Healthcare. |
| Pharmaceutical Class | Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA019829 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 17156-0022-05 (17156002205)
| NDC Package Code | 17156-022-05 |
|---|---|
| Billing NDC | 17156002205 |
| Package | 5 VIAL in 1 TRAY (17156-022-05) / 5 mL in 1 VIAL |
| Marketing Start Date | 1988-12-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |