OTC
Strength
200; 30 mg/1; mg/1
Manufacturer
Haleon US Holdings LLCNDC
00573018021
Classification
Brand
Dosage Form
TABLET, COATED
Route
ORAL
Last Updated
10/21/2015
Active Ingredients
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA019771On Market Since
9/19/1989
Pharmacological Classes
Adrenergic alpha-Agonists
Anti-Inflammatory Agents
Non-Steroidal
Cyclooxygenase Inhibitors
Nonsteroidal Anti-inflammatory Drug
alpha-Adrenergic Agonist
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