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: A077314
Product Number: 001
Approval Date: Sep 15, 2005
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information