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Sodium Tetradecyl Sulfate

NDC 24201-201 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209937
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM TETRADECYL SULFATE (30 mg/mL)
Marketing started20191209
Package count1

External sources

Source: openFDA. Public-domain (CC0).