FDA NDC
Oxymorphone hydrochloride
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 0115-1315
- Proprietary name
- Oxymorphone hydrochloride
- Nonproprietary name
- Oxymorphone hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Strength
- 7.5 mg/1
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