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
- 71335-1959_6eeeb7dc-4dfc-4cb4-99cf-ffcee9112f00
- Product NDC
- 71335-1959
- 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 — 7.5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET in 1 BOTTLE (71335-1959-1) · 71335-1959-1
- 36 TABLET in 1 BOTTLE (71335-1959-2) · 71335-1959-2
- 20 TABLET in 1 BOTTLE (71335-1959-3) · 71335-1959-3
- 30 TABLET in 1 BOTTLE (71335-1959-4) · 71335-1959-4
- 45 TABLET in 1 BOTTLE (71335-1959-5) · 71335-1959-5
- 60 TABLET in 1 BOTTLE (71335-1959-6) · 71335-1959-6
- 90 TABLET in 1 BOTTLE (71335-1959-7) · 71335-1959-7
- 120 TABLET in 1 BOTTLE (71335-1959-8) · 71335-1959-8
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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