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Ketamine Hydrochloride
Ketamine Hydrochloride - 0409-2051-05 - (KETAMINE HYDROCHLORIDE)
Drug Information of Ketamine Hydrochloride
| Product NDC: | 0409-2051 |
| Proprietary Name: | Ketamine Hydrochloride |
| Non Proprietary Name: | KETAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 100 mg/mL & nbsp; KETAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketamine Hydrochloride
| Product NDC: | 0409-2051 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074549 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960627 |
Package Information of Ketamine Hydrochloride
| Package NDC: | 0409-2051-05 |
| Package Description: | 10 VIAL, MULTI-DOSE in 1 BOX (0409-2051-05) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Ketamine Hydrochloride
| NDC Code | 0409-2051-05 |
| Proprietary Name | Ketamine Hydrochloride |
| Package Description | 10 VIAL, MULTI-DOSE in 1 BOX (0409-2051-05) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0409-2051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | KETAMINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19960627 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | KETAMINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
