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Ketamine Hydrochloride
Ketamine Hydrochloride - 67457-001-10 - (Ketamine Hydrochloride)
Drug Information of Ketamine Hydrochloride
| Product NDC: | 67457-001 |
| Proprietary Name: | Ketamine Hydrochloride |
| Non Proprietary Name: | Ketamine Hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Ketamine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketamine Hydrochloride
| Product NDC: | 67457-001 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076092 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130604 |
Package Information of Ketamine Hydrochloride
| Package NDC: | 67457-001-10 |
| Package Description: | 10 VIAL in 1 CARTON (67457-001-10) > 10 mL in 1 VIAL (67457-001-00) |
NDC Information of Ketamine Hydrochloride
| NDC Code | 67457-001-10 |
| Proprietary Name | Ketamine Hydrochloride |
| Package Description | 10 VIAL in 1 CARTON (67457-001-10) > 10 mL in 1 VIAL (67457-001-00) |
| Product NDC | 67457-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketamine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20130604 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | KETAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
