FDA.reportPublic FDA data

Oxycodone Hydrochloride

Product NDC
72162-1811
11-digit product format
721621811
Labeler code
72162
Product ID
72162-1811_c990c114-53b0-4621-9a31-c31ba43f6527
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
5 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 HYDROCHLORIDE5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC1ENJ2TE6C
Rxcui1049621

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1811-0Oxycodone Hydrochloride30 in 1 BOTTLETABLET30101
72162-1811-1Oxycodone Hydrochloride60 in 1 BOTTLETABLET60101
72162-1811-2Oxycodone Hydrochloride90 in 1 BOTTLETABLET90101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1811-0EA - Each72162-181183d6935b-2039-47c8-9896-06412a9fa1f512023-10-16
72162-1811-1EA - Each72162-1811e18fe73e-2cf6-4495-9a21-36544df4d7c212023-10-16
72162-1811-2EA - Each72162-181125d1dd65-9fc6-42eb-a85b-c811ce3ee90c12023-10-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1811OXYCODONE HYDROCHLORIDE (OXYCODONE) TABLET [BRYANT RANCH PREPACK]101Current NDC, 3 package rows20240601_bc7fdf7e-ad4e-4a04-b35c-2233cc7e5f15.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049621oxyCODONE HCl 5 MG Oral TabletPSNbc7fdf7e-ad4e-4a04-b35c-2233cc7e5f15101
1049621oxycodone hydrochloride 5 MG Oral TabletSCDbc7fdf7e-ad4e-4a04-b35c-2233cc7e5f15101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1811-07216218110030 TABLET in 1 BOTTLE (72162-1811-0) 30 tablet2024-05-30NoNoCurrent
72162-1811-17216218110160 TABLET in 1 BOTTLE (72162-1811-1) 60 tablet2024-05-30NoNoCurrent
72162-1811-27216218110290 TABLET in 1 BOTTLE (72162-1811-2) 90 tablet2024-05-30NoNoCurrent