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ketamine hydrochloride - 42023-138-10 - (ketamine hydrochloride)

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Drug Information of ketamine hydrochloride

Product NDC: 42023-138
Proprietary Name: ketamine hydrochloride
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 ketamine hydrochloride

Product NDC: 42023-138
Labeler Name: JHP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016812
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120601

Package Information of ketamine hydrochloride

Package NDC: 42023-138-10
Package Description: 10 VIAL in 1 CARTON (42023-138-10) > 10 mL in 1 VIAL

NDC Information of ketamine hydrochloride

NDC Code 42023-138-10
Proprietary Name ketamine hydrochloride
Package Description 10 VIAL in 1 CARTON (42023-138-10) > 10 mL in 1 VIAL
Product NDC 42023-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketamine hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120601
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name JHP Pharmaceuticals, LLC
Substance Name KETAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of ketamine hydrochloride


General Information