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Hydromorphone Hydrochloride

NDC 0406-3243 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehydromorphone hydrochloride
Labeler / ManufacturerSpecGx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076855
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROMORPHONE HYDROCHLORIDE (2 mg/1)
Marketing started20041223
Package count1

External sources

Source: openFDA. Public-domain (CC0).