FDA NDC Directory · JSON-LD · Markdown

Zinc Sulfate

NDC 68083-608 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216249
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsZINC SULFATE (1 mg/mL)
Marketing started20230901
Package count1

External sources

Source: openFDA. Public-domain (CC0).