Strength
9 mg/mL
Manufacturer
Nephron Pharmaceuticals CorporationNDC
00487430110
Classification
Generic
Dosage Form
INJECTION
Route
INTRAVENOUS
Last Updated
7/23/2025
Active Ingredients
SODIUM CHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA211968On Market Since
6/4/2020
SODIUM CHLORIDE 0.9% SOLUTION
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SODIUM CHLORIDE 0.9% SOLUTION
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SODIUM CHLORIDE 0.9% VIAL
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SODIUM CHLORIDE 0.9% VIAL
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