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Product Details for NDA 212535

NOURESS (CYSTEINE HYDROCHLORIDE)
500MG/10ML (50MG/ML)
Marketing Status: Discontinued
Active Ingredient: CYSTEINE HYDROCHLORIDE
Proprietary Name: NOURESS
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 500MG/10ML (50MG/ML)
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N212535
Product Number: 001
Approval Date: Dec 13, 2019
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:  Discontinued
Patent and Exclusivity Information
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