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
- 63629-8834_71adc4c3-b213-43de-8074-fdc2c2bed2b3
- Product NDC
- 63629-8834
- 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 (63629-8834-1) · 63629-8834-1
- 120 TABLET in 1 BOTTLE (63629-8834-2) · 63629-8834-2
- 90 TABLET in 1 BOTTLE (63629-8834-3) · 63629-8834-3
- 28 TABLET in 1 BOTTLE (63629-8834-4) · 63629-8834-4
- 60 TABLET in 1 BOTTLE (63629-8834-5) · 63629-8834-5
- 20 TABLET in 1 BOTTLE (63629-8834-6) · 63629-8834-6
- 45 TABLET in 1 BOTTLE (63629-8834-7) · 63629-8834-7
- 75 TABLET in 1 BOTTLE (63629-8834-8) · 63629-8834-8
- 100 TABLET in 1 BOTTLE (63629-8834-9) · 63629-8834-9
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 →