KETALAR - 52584-037-10 - (ketamine hydrochloride)

Alphabetical Index


Drug Information of KETALAR

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)

Labeler Information of KETALAR

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 Information of KETALAR

Package NDC: 52584-037-10
Package Description: 1 VIAL in 1 BAG (52584-037-10) > 20 mL in 1 VIAL

NDC Information of KETALAR

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]

Complete Information of KETALAR


General Information