Active Ingredient: DOBUTAMINE HYDROCHLORIDE
Proprietary Name: DOBUTAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 12.5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074545
Product Number: 001
Approval Date: Jun 25, 1998
Applicant Holder Full Name: LUITPOLD PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information