Propofol - 0703-2856-04 - (Propofol)

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Drug Information of Propofol

Product NDC: 0703-2856
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: 0703-2856
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075102
Marketing Category: ANDA
Start Marketing Date: 20070621

Package Information of Propofol

Package NDC: 0703-2856-04
Package Description: 25 VIAL, SINGLE-USE in 1 TRAY (0703-2856-04) > 20 mL in 1 VIAL, SINGLE-USE (0703-2856-01)

NDC Information of Propofol

NDC Code 0703-2856-04
Proprietary Name Propofol
Package Description 25 VIAL, SINGLE-USE in 1 TRAY (0703-2856-04) > 20 mL in 1 VIAL, SINGLE-USE (0703-2856-01)
Product NDC 0703-2856
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propofol
Dosage Form Name INJECTION, EMULSION
Route Name INTRAVENOUS
Start Marketing Date 20070621
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc.
Substance Name PROPOFOL
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Propofol


General Information