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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020441

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PULMICORT (BUDESONIDE)
0.16MG/INH
Marketing Status: Discontinued
Active Ingredient: BUDESONIDE
Proprietary Name: PULMICORT
Dosage Form; Route of Administration: POWDER, METERED; INHALATION
Strength: 0.16MG/INH
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020441
Product Number: 002
Approval Date: Jun 24, 1997
Applicant Holder Full Name: ASTRAZENECA PHARMACEUTICALS LP
Marketing Status:  Discontinued
Patent and Exclusivity Information
PULMICORT (BUDESONIDE)
0.32MG/INH
Marketing Status: Discontinued
Active Ingredient: BUDESONIDE
Proprietary Name: PULMICORT
Dosage Form; Route of Administration: POWDER, METERED; INHALATION
Strength: 0.32MG/INH
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020441
Product Number: 003
Approval Date: Jun 24, 1997
Applicant Holder Full Name: ASTRAZENECA PHARMACEUTICALS LP
Marketing Status:  Discontinued
Patent and Exclusivity Information
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