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
- 71930-022_d5dbbf3c-6269-488c-b3a2-9539f45e3945
- Product NDC
- 71930-022
- Form
- SOLUTION
- Composition / generic term
- Oxycodone Hydrochloride
- Labeler
- Eywa Pharma Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190301
- Source listing expiry
- 20271231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (71930-022-43) / 473 mL in 1 BOTTLE · 71930-022-43
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →