Active Ingredient: GUAIFENESIN; HYDROCODONE BITARTRATE
Proprietary Name: XTRELUS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG;5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N208085
Product Number: 001
Approval Date: Apr 25, 2018
Applicant Holder Full Name: ECI PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information