United States · FDA National Drug Code directory
Oxymorphone hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0115-1315_a8dc6624-df1e-4e5a-b445-9541658e3430
- Product NDC
- 0115-1315
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Oxymorphone hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130102
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYMORPHONE HYDROCHLORIDE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-01) · 0115-1315-01
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-03) · 0115-1315-03
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-08) · 0115-1315-08
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-13) · 0115-1315-13
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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