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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074332

BUMETANIDE (BUMETANIDE)
0.25MG/ML
Marketing Status: Prescription
Active Ingredient: BUMETANIDE
Proprietary Name: BUMETANIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.25MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A074332
Product Number: 001
Approval Date: Oct 31, 1994
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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