Active Ingredient: GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 600MG;60MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A216082
Product Number: 001
Approval Date: Aug 22, 2022
Applicant Holder Full Name: GRANULES INDIA LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 1.2GM;120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A216082
Product Number: 002
Approval Date: Aug 22, 2022
Applicant Holder Full Name: GRANULES INDIA LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information