FDA NDC Directory · JSON-LD · Markdown

Zinc sulfate

NDC 70069-692 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216135
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsZINC SULFATE (3 mg/mL)
Marketing started20240718
Package count1

External sources

Source: openFDA. Public-domain (CC0).