United States · FDA National Drug Code directory
OXYCODONE AND ACETAMINOPHEN
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
- 71335-2106_3e2312f9-2b0c-4137-88e2-5c75c659a6d0
- Product NDC
- 71335-2106
- Form
- TABLET
- Composition / generic term
- Oxycodone and Acetaminophen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170411
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 10 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2106-1) · 71335-2106-1
- 120 TABLET in 1 BOTTLE (71335-2106-2) · 71335-2106-2
- 90 TABLET in 1 BOTTLE (71335-2106-3) · 71335-2106-3
- 28 TABLET in 1 BOTTLE (71335-2106-4) · 71335-2106-4
- 60 TABLET in 1 BOTTLE (71335-2106-5) · 71335-2106-5
- 20 TABLET in 1 BOTTLE (71335-2106-6) · 71335-2106-6
- 45 TABLET in 1 BOTTLE (71335-2106-7) · 71335-2106-7
- 75 TABLET in 1 BOTTLE (71335-2106-8) · 71335-2106-8
- 100 TABLET in 1 BOTTLE (71335-2106-9) · 71335-2106-9
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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