High Outlier
OTC
Strength
200 mg/1
Manufacturer
Haleon US Holdings LLCNDC
00573016151
Classification
Brand
Dosage Form
TABLET, COATED
Route
ORAL
Last Updated
11/18/2015
Active Ingredients
IBUPROFENApproval Type
New Drug (NDA)
FDA Application
NDA018989On Market Since
5/18/1984
Pharmacological Classes
Related Drugs
Same classification
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