Active Ingredient: RITODRINE HYDROCHLORIDE
Proprietary Name: RITODRINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071188
Product Number: 001
Approval Date: Jul 23, 1987
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information