Ethamolin - 67871-479-06 - (Ethanolamine Oleate)

Alphabetical Index


Drug Information of Ethamolin

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)

Labeler Information of Ethamolin

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 Information of Ethamolin

Package NDC: 67871-479-06
Package Description: 10 AMPULE in 1 BOX (67871-479-06) > 2 mL in 1 AMPULE

NDC Information of Ethamolin

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]

Complete Information of Ethamolin


General Information