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Active Ingredient: CHLOROTHIAZIDE SODIUM
Proprietary Name: CHLOROTHIAZIDE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A090896
Product Number: 001
Approval Date: Oct 16, 2009
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information