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Sodium Chloride

NDC 70512-841 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSOLA Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207956
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (9 g/1000mL)
Marketing started20170525
Package count5

External sources

Source: openFDA. Public-domain (CC0).