| Product NDC: | 52584-037 |
| Proprietary Name: | KETALAR |
| Non Proprietary Name: | ketamine hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; ketamine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52584-037 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016812 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121017 |
| Package NDC: | 52584-037-10 |
| Package Description: | 1 VIAL in 1 BAG (52584-037-10) > 20 mL in 1 VIAL |
| NDC Code | 52584-037-10 |
| Proprietary Name | KETALAR |
| Package Description | 1 VIAL in 1 BAG (52584-037-10) > 20 mL in 1 VIAL |
| Product NDC | 52584-037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketamine hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20121017 |
| Marketing Category Name | NDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | KETAMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |