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CERETEC
CERETEC - 17156-022-05 - (exametazime)
Drug Information of CERETEC
| Product NDC: | 17156-022 |
| Proprietary Name: | CERETEC |
| Non Proprietary Name: | exametazime |
| Active Ingredient(s): | .5 mg/5mL & nbsp; exametazime |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CERETEC
| Product NDC: | 17156-022 |
| Labeler Name: | Medi-Physics Inc. dba GE Healthcare. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019829 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19881230 |
Package Information of CERETEC
| Package NDC: | 17156-022-05 |
| Package Description: | 5 VIAL in 1 KIT (17156-022-05) > 5 mL in 1 VIAL |
NDC Information of CERETEC
| NDC Code | 17156-022-05 |
| Proprietary Name | CERETEC |
| Package Description | 5 VIAL in 1 KIT (17156-022-05) > 5 mL in 1 VIAL |
| Product NDC | 17156-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | exametazime |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19881230 |
| Marketing Category Name | NDA |
| Labeler Name | Medi-Physics Inc. dba GE Healthcare. |
| Substance Name | EXAMETAZIME |
| Strength Number | .5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
