FDA NDC Directory · JSON-LD · Markdown

Humatin

NDC 80725-250 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namePAROMOMYCIN SULFATE
Labeler / ManufacturerWaylis Therapeutics LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065173
Dosage form / routeCAPSULE · ORAL
Active ingredientsPAROMOMYCIN SULFATE (250 mg/1)
Marketing started20210408
Package count1

External sources

Source: openFDA. Public-domain (CC0).