Product NDC: | 42023-113 |
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: | 42023-113 |
Labeler Name: | JHP Pharmaceuticals LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016812 |
Marketing Category: | NDA |
Start Marketing Date: | 20071001 |
Package NDC: | 42023-113-10 |
Package Description: | 10 VIAL in 1 CARTON (42023-113-10) > 20 mL in 1 VIAL |
NDC Code | 42023-113-10 |
Proprietary Name | Ketalar |
Package Description | 10 VIAL in 1 CARTON (42023-113-10) > 20 mL in 1 VIAL |
Product NDC | 42023-113 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ketamine hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20071001 |
Marketing Category Name | NDA |
Labeler Name | JHP Pharmaceuticals LLC |
Substance Name | KETAMINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |