Ultane - 0074-4456-04 - (Sevoflurane)

Alphabetical Index


Drug Information of Ultane

Product NDC: 0074-4456
Proprietary Name: Ultane
Non Proprietary Name: Sevoflurane
Active Ingredient(s): 250    mL/250mL & nbsp;   Sevoflurane
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ultane

Product NDC: 0074-4456
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020478
Marketing Category: NDA
Start Marketing Date: 19950607

Package Information of Ultane

Package NDC: 0074-4456-04
Package Description: 250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)

NDC Information of Ultane

NDC Code 0074-4456-04
Proprietary Name Ultane
Package Description 250 mL in 1 BOTTLE, PLASTIC (0074-4456-04)
Product NDC 0074-4456
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sevoflurane
Dosage Form Name LIQUID
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19950607
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name SEVOFLURANE
Strength Number 250
Strength Unit mL/250mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Ultane


General Information