Propofol - 63323-270-67 - (PROPOFOL)

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Drug Information of Propofol

Product NDC: 63323-270
Proprietary Name: Propofol
Non Proprietary Name: PROPOFOL
Active Ingredient(s): 10    mg/mL & nbsp;   PROPOFOL
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Propofol

Product NDC: 63323-270
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019627
Marketing Category: NDA
Start Marketing Date: 20091007

Package Information of Propofol

Package NDC: 63323-270-67
Package Description: 10 VIAL in 1 BOX (63323-270-67) > 100 mL in 1 VIAL

NDC Information of Propofol

NDC Code 63323-270-67
Proprietary Name Propofol
Package Description 10 VIAL in 1 BOX (63323-270-67) > 100 mL in 1 VIAL
Product NDC 63323-270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROPOFOL
Dosage Form Name INJECTION, EMULSION
Route Name INTRAVENOUS
Start Marketing Date 20091007
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name PROPOFOL
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Propofol


General Information