Product NDC: | 0409-6695 |
Proprietary Name: | Amidate |
Non Proprietary Name: | ETOMIDATE |
Active Ingredient(s): | 2 mg/mL & nbsp; ETOMIDATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-6695 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018227 |
Marketing Category: | NDA |
Start Marketing Date: | 20100210 |
Package NDC: | 0409-6695-02 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0409-6695-02 |
Proprietary Name | Amidate |
Package Description | 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) > 20 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0409-6695 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ETOMIDATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100210 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | ETOMIDATE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |