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Hydrocortisone sodium succinate

NDC 70710-1907 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217191
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsHYDROCORTISONE SODIUM SUCCINATE (100 mg/2mL)
Marketing started20260509
Package count1

External sources

Source: openFDA. Public-domain (CC0).