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