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KETAMINE HYDROCHLORIDE
KETAMINE HYDROCHLORIDE - 52584-040-05 - (ketamine hydrochloride)
Drug Information of KETAMINE HYDROCHLORIDE
| Product NDC: | 52584-040 |
| 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: | 52584-040 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074549 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121016 |
Package Information of KETAMINE HYDROCHLORIDE
| Package NDC: | 52584-040-05 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BAG (52584-040-05) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Information of KETAMINE HYDROCHLORIDE
| NDC Code | 52584-040-05 |
| Proprietary Name | KETAMINE HYDROCHLORIDE |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (52584-040-05) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 52584-040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketamine hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20121016 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | KETAMINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
