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Ketalar
Ketalar - 42023-114-10 - (ketamine hydrochloride)
Drug Information of Ketalar
| Product NDC: | 42023-114 |
| Proprietary Name: | Ketalar |
| Non Proprietary Name: | ketamine hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; ketamine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketalar
| Product NDC: | 42023-114 |
| Labeler Name: | JHP Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016812 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071001 |
Package Information of Ketalar
| Package NDC: | 42023-114-10 |
| Package Description: | 10 VIAL in 1 CARTON (42023-114-10) > 10 mL in 1 VIAL |
NDC Information of Ketalar
| NDC Code | 42023-114-10 |
| Proprietary Name | Ketalar |
| Package Description | 10 VIAL in 1 CARTON (42023-114-10) > 10 mL in 1 VIAL |
| Product NDC | 42023-114 |
| 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 | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
