FDA NDC Directory · JSON-LD · Markdown

Zinc Sulfate

NDC 0517-6103 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerAmerican Regent, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA209377
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsZINC SULFATE (3 mg/mL)
Marketing started20191001
Package count1

External sources

Source: openFDA. Public-domain (CC0).