FDA NDC Directory · JSON-LD · Markdown

Phentolamine Mesylate

NDC 0143-9564 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040235
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsPHENTOLAMINE MESYLATE (5 mg/mL)
Marketing started19980515
Package count2

External sources

Source: openFDA. Public-domain (CC0).