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Ketamine Hydrochloride - 67457-181-20 - (Ketamine Hydrochloride)

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Drug Information of Ketamine Hydrochloride

Product NDC: 67457-181
Proprietary Name: Ketamine Hydrochloride
Non Proprietary Name: Ketamine Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Ketamine Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ketamine Hydrochloride

Product NDC: 67457-181
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076092
Marketing Category: ANDA
Start Marketing Date: 20130604

Package Information of Ketamine Hydrochloride

Package NDC: 67457-181-20
Package Description: 10 VIAL in 1 CARTON (67457-181-20) > 20 mL in 1 VIAL (67457-181-00)

NDC Information of Ketamine Hydrochloride

NDC Code 67457-181-20
Proprietary Name Ketamine Hydrochloride
Package Description 10 VIAL in 1 CARTON (67457-181-20) > 20 mL in 1 VIAL (67457-181-00)
Product NDC 67457-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketamine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20130604
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name KETAMINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Ketamine Hydrochloride


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