United States · FDA National Drug Code directory
Oxycodone 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
- 42858-001_d95a9c89-1435-4594-be8b-e19e23d07c0a
- Product NDC
- 42858-001
- Form
- TABLET
- Composition / generic term
- Oxycodone Hydrochloride
- Labeler
- Rhodes Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140908
- Source listing expiry
- 20271231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (42858-001-01) · 42858-001-01
- 10 BLISTER PACK in 1 CARTON (42858-001-10) / 10 TABLET in 1 BLISTER PACK · 42858-001-10
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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