Optison - 0407-2707-03 - (Human Albumin Microspheres)

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Drug Information of Optison

Product NDC: 0407-2707
Proprietary Name: Optison
Non Proprietary Name: Human Albumin Microspheres
Active Ingredient(s): 10    mg/mL & nbsp;   Human Albumin Microspheres
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Optison

Product NDC: 0407-2707
Labeler Name: GE Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020899
Marketing Category: NDA
Start Marketing Date: 20020102

Package Information of Optison

Package NDC: 0407-2707-03
Package Description: 5 VIAL, SINGLE-USE in 1 CARTON (0407-2707-03) > 3 mL in 1 VIAL, SINGLE-USE

NDC Information of Optison

NDC Code 0407-2707-03
Proprietary Name Optison
Package Description 5 VIAL, SINGLE-USE in 1 CARTON (0407-2707-03) > 3 mL in 1 VIAL, SINGLE-USE
Product NDC 0407-2707
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Human Albumin Microspheres
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020102
Marketing Category Name NDA
Labeler Name GE Healthcare Inc.
Substance Name HUMAN ALBUMIN MICROSPHERES
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Contrast Agent for Ultrasound Imaging [EPC],Ultrasound Contrast Activity [MoA]

Complete Information of Optison


General Information