Active Ingredient: NIZATIDINE
Proprietary Name: NIZATIDINE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090618
Product Number: 001
Approval Date: Jul 15, 2011
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS INC USA
Marketing Status:
Prescription
Patent and Exclusivity Information