Active Ingredient: BENZONATATE
Proprietary Name: BENZONATATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040587
Product Number: 001
Approval Date: Mar 19, 2008
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
