NDCFind

6% Hetastarch In 0.9% Sodium Chloride 51662-1317

Product NDC

51662-1317
Manufacturer
Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form
Injection, Solution
Route
Intravenous
Product Type
Human Prescription Drug
Marketing Start
November 26, 2018
Listing Expires
December 31, 2026
Application
BA740193
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Active Ingredients

IngredientStrength
Hetastarch6 g/100mL

Drug Class

Plasma Volume Expander [EPC]Increased Intravascular Volume [PE]Osmotic Activity [MoA]

Packaging Options(2)

500 mL in 1 CONTAINER (51662-1317-1)

12 CONTAINER in 1 CASE (51662-1317-3) / 500 mL in 1 CONTAINER (51662-1317-2)