High Outlier
Strength
750 mg/5mL
Manufacturer
GlaxoSmithKline LLCNDC
00173054700
Classification
Brand
Dosage Form
SUSPENSION
Route
ORAL
Last Updated
1/1/2019
Active Ingredients
ATOVAQUONEApproval Type
New Drug (NDA)
FDA Application
NDA020500On Market Since
9/18/1998
Pharmacological Classes
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