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] |