Active Ingredient: DESMOPRESSIN ACETATE
Proprietary Name: DESMOPRESSIN ACETATE
Dosage Form; Route of Administration: SOLUTION; NASAL
Strength: 0.01%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077212
Product Number: 001
Approval Date: Apr 12, 2012
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information