Active Ingredient: TIZANIDINE HYDROCHLORIDE
Proprietary Name: TIZANIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076354
Product Number: 001
Approval Date: Mar 28, 2003
Applicant Holder Full Name: RISING PHARMA HOLDING INC
Marketing Status:
Discontinued
Patent and Exclusivity Information