Active Ingredient: MECLIZINE HYDROCHLORIDE
Proprietary Name: MECLIZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085269
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information