FDA.reportPublic FDA data

Oxycodone Hydrochloride

Product NDC
71335-1023
11-digit product format
713351023
Labeler code
71335
Product ID
71335-1023_09003109-fe5e-4830-923b-869e60b5cfc4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203638
Marketing category
ANDA
Marketing start
2012-10-30
Substance
OXYCODONE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Oxycodone Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OXYCODONE HYDROCHLORIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC1ENJ2TE6C
Rxcui1049686

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
92ead9ae-674d-4eee-a492-c385d496891fProduct name320220308
b8cd3792-f010-440e-ac63-7713119fde04Product name920220110
bde672ba-4805-28d0-1986-73543d41b412Product name220210201
b8497372-efe9-9dde-fa2d-59be9761aa64Product name920200428
ac683e31-73f8-f1cd-ff51-87d7b0d20ab3Product name920190611
2a0c98e1-033f-4e0d-a0da-b5291ffbe880Product name120190320
b7a189a6-82e9-f884-a16b-8cdc7e7d1556Product name620170913
5da64f4c-1e90-423d-af7a-5a52bb3e823eProduct name420170726
334cd9e0-ccc1-4fe7-b3a9-7d5942867ee6Product name120170628
8e48b6b8-3a2f-4e0d-b7c9-38d70393b778Product name120161103
68d3ff71-7803-4cf4-ba84-71ce4712df22Product name120160620
07e5b999-fda7-79c9-8f77-8380537ade79Product name420160517
8a245632-e24f-4ccc-b671-995d89c96ebcProduct name120141203
23475c0b-a5b5-4fec-b97f-acca901eae6aProduct name120140718
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
7fa873c5-fb27-7119-0a05-634ad477dea7Product name120140508
c8753a88-edde-8e17-a396-705537b52ceeProduct name120140508
cd4f9ae2-1343-ecd2-ce0f-97db0c2b51ceProduct name120140508
cf3a804d-0326-aa22-0142-c184b5657d85Product name120140508
f46484d2-0de6-24f4-bf73-a8f2af6723efProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71335-1023-12024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-22024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-32024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-42024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-52024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-62024-05-31C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-12024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-22024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-32024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-42024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-52024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950
71335-1023-62024-01-30C16284748780-11030e365-18ad-111a-e063-dadaa90a10e2These highlights do not include all the information needed to use OXYCODONE HCl TABLETS safely and effectively. See full prescribing information for OXYCODONE HCl TABLETS. OXYCODONE HCl tablets, for oral use, CII Initial U.S. Approval: 1950

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1023-1Oxycodone Hydrochloride60 in 1 BOTTLETABLET60101
71335-1023-2Oxycodone Hydrochloride90 in 1 BOTTLETABLET90101
71335-1023-3Oxycodone Hydrochloride28 in 1 BOTTLETABLET28101
71335-1023-4Oxycodone Hydrochloride30 in 1 BOTTLETABLET30101
71335-1023-5Oxycodone Hydrochloride8 in 1 BOTTLETABLET8101
71335-1023-6Oxycodone Hydrochloride6 in 1 BOTTLETABLET6101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1023OXYCODONE HYDROCHLORIDE (OXYCODONE) TABLET [BRYANT RANCH PREPACK]101Current NDC, Legacy NDC, 6 package rows20240602_b2510d72-bf63-4c9d-ac5e-7bacd993fa10.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049686oxyCODONE HCl 20 MG Oral TabletPSNb2510d72-bf63-4c9d-ac5e-7bacd993fa10101
1049686oxycodone hydrochloride 20 MG Oral TabletSCDb2510d72-bf63-4c9d-ac5e-7bacd993fa10101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1023-17133510230160 TABLET in 1 BOTTLE (71335-1023-1) 60 tablet2018-12-070000-00-00NoNoCurrent
71335-1023-27133510230290 TABLET in 1 BOTTLE (71335-1023-2) 90 tablet2024-05-300000-00-00NoNoCurrent
71335-1023-37133510230328 TABLET in 1 BOTTLE (71335-1023-3) 28 tablet2024-05-300000-00-00NoNoCurrent
71335-1023-47133510230430 TABLET in 1 BOTTLE (71335-1023-4) 30 tablet2020-02-250000-00-00NoNoCurrent
71335-1023-5713351023058 TABLET in 1 BOTTLE (71335-1023-5) 8 tablet2024-05-300000-00-00NoNoCurrent
71335-1023-6713351023066 TABLET in 1 BOTTLE (71335-1023-6) 6 tablet2024-05-300000-00-00NoNoCurrent