Active Ingredient: METOCLOPRAMIDE HYDROCHLORIDE
Proprietary Name: METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072436
Product Number: 001
Approval Date: Jun 22, 1989
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Discontinued
Patent and Exclusivity Information