Product NDC: | 67871-479 |
Proprietary Name: | Ethamolin |
Non Proprietary Name: | Ethanolamine Oleate |
Active Ingredient(s): | 50 mg/mL & nbsp; Ethanolamine Oleate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67871-479 |
Labeler Name: | QOL Medical, LLC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019357 |
Marketing Category: | NDA |
Start Marketing Date: | 19981222 |
Package NDC: | 67871-479-06 |
Package Description: | 10 AMPULE in 1 BOX (67871-479-06) > 2 mL in 1 AMPULE |
NDC Code | 67871-479-06 |
Proprietary Name | Ethamolin |
Package Description | 10 AMPULE in 1 BOX (67871-479-06) > 2 mL in 1 AMPULE |
Product NDC | 67871-479 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ethanolamine Oleate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19981222 |
Marketing Category Name | NDA |
Labeler Name | QOL Medical, LLC. |
Substance Name | ETHANOLAMINE OLEATE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sclerosing Activity [MoA],Sclerosing Agent [EPC],Vascular Sclerosing Activity [PE] |