Ketalar - 42023-113-10 - (ketamine hydrochloride)

Alphabetical Index


Drug Information of Ketalar

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)

Labeler Information of Ketalar

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 Information of Ketalar

Package NDC: 42023-113-10
Package Description: 10 VIAL in 1 CARTON (42023-113-10) > 20 mL in 1 VIAL

NDC Information of Ketalar

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]

Complete Information of Ketalar


General Information