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Hydrocortisone sodium succinate

NDC 60505-6411 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA219856
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsHYDROCORTISONE SODIUM SUCCINATE (100 mg/2mL)
Marketing started20260619
Package count1

External sources

Source: openFDA. Public-domain (CC0).