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Brevital Sodium - 42023-105-01 - (methohexital sodium)

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Drug Information of Brevital Sodium

Product NDC: 42023-105
Proprietary Name: Brevital Sodium
Non Proprietary Name: methohexital sodium
Active Ingredient(s): 500    mg/1 & nbsp;   methohexital sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; RECTAL
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Brevital Sodium

Product NDC: 42023-105
Labeler Name: JHP Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011559
Marketing Category: NDA
Start Marketing Date: 20071101

Package Information of Brevital Sodium

Package NDC: 42023-105-01
Package Description: 1 VIAL in 1 CARTON (42023-105-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

NDC Information of Brevital Sodium

NDC Code 42023-105-01
Proprietary Name Brevital Sodium
Package Description 1 VIAL in 1 CARTON (42023-105-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Product NDC 42023-105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methohexital sodium
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; RECTAL
Start Marketing Date 20071101
Marketing Category Name NDA
Labeler Name JHP Pharmaceuticals LLC
Substance Name METHOHEXITAL SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Barbiturate [EPC],Barbiturates [Chemical/Ingredient]

Complete Information of Brevital Sodium


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