Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: ZANTAC 150
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020095
Product Number: 001
Approval Date: Mar 8, 1994
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information