FDA NDC Directory · JSON-LD · Markdown

Hydromorphone Hydrochloride

NDC 63323-852 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryNew Drug Application (innovator) · App NDA019034
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsHYDROMORPHONE HYDROCHLORIDE (1 mg/mL)
Marketing started20171215
Package count1

External sources

Source: openFDA. Public-domain (CC0).