Active Ingredient: GUAIFENESIN
Proprietary Name: GUAIFENESIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A207342
Product Number: 001
Approval Date: Jul 11, 2018
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS OF NEW YORK LLC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information