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Precedex
Precedex - 0409-1638-02 - (DEXMEDETOMIDINE HYDROCHLORIDE)
Drug Information of Precedex
| Product NDC: | 0409-1638 |
| Proprietary Name: | Precedex |
| Non Proprietary Name: | DEXMEDETOMIDINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 ug/mL & nbsp; DEXMEDETOMIDINE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Precedex
| Product NDC: | 0409-1638 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021038 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19991217 |
Package Information of Precedex
| Package NDC: | 0409-1638-02 |
| Package Description: | 25 VIAL in 1 TRAY (0409-1638-02) > 2 mL in 1 VIAL |
NDC Information of Precedex
| NDC Code | 0409-1638-02 |
| Proprietary Name | Precedex |
| Package Description | 25 VIAL in 1 TRAY (0409-1638-02) > 2 mL in 1 VIAL |
| Product NDC | 0409-1638 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXMEDETOMIDINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19991217 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DEXMEDETOMIDINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC],General Anesthesia [PE] |
