Active Ingredient: CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: ZUTRIPRO
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 4MG/5ML;5MG/5ML;60MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N022439
Product Number: 001
Approval Date: Jun 8, 2011
Applicant Holder Full Name: PERSION PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
