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Active Ingredient: BUDESONIDE
Proprietary Name: BUDESONIDE
Dosage Form; Route of Administration: SUSPENSION; INHALATION
Strength: 0.25MG/2ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AN
Application Number: A077519
Product Number: 001
Approval Date: Nov 18, 2008
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: BUDESONIDE
Proprietary Name: BUDESONIDE
Dosage Form; Route of Administration: SUSPENSION; INHALATION
Strength: 0.5MG/2ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AN
Application Number: A077519
Product Number: 002
Approval Date: Nov 18, 2008
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information