FDA.reportPublic FDA data

Oxycodone Hydrochloride

Product NDC
63629-8890
11-digit product format
636298890
Labeler code
63629
Product ID
63629-8890_9b4726e8-108a-4df5-aad5-02af0fb8ef6b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207418
Marketing category
ANDA
Marketing start
2017-08-08
Substance
OXYCODONE HYDROCHLORIDE
Active strength
30 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Oxycodone Hydrochloride
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OXYCODONE HYDROCHLORIDE30 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC1ENJ2TE6C
Rxcui1049618

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
63629-8890-1Oxycodone Hydrochloride30 in 1 BOTTLETABLET30102
63629-8890-2Oxycodone Hydrochloride60 in 1 BOTTLETABLET60102
63629-8890-3Oxycodone Hydrochloride90 in 1 BOTTLETABLET90102
63629-8890-4Oxycodone Hydrochloride120 in 1 BOTTLETABLET120102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-8890-1EA - Each63629-8890913ebf73-1106-4ccc-8970-cbd481792f1312022-11-07
63629-8890-2EA - Each63629-8890cc976a07-4928-42a1-ab8f-d5f8c6f0798312022-11-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-8890OXYCODONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]101Current NDC, Legacy NDC, 4 package rows20231027_ff7f1268-ddb7-4742-beee-8b12966fe8f9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049618oxyCODONE HCl 30 MG Oral TabletPSNff7f1268-ddb7-4742-beee-8b12966fe8f9102
1049618oxycodone hydrochloride 30 MG Oral TabletSCDff7f1268-ddb7-4742-beee-8b12966fe8f9102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-8890-16362988900130 TABLET in 1 BOTTLE (63629-8890-1) 30 tablet2021-10-110000-00-00NoNoCurrent
63629-8890-26362988900260 TABLET in 1 BOTTLE (63629-8890-2) 60 tablet2021-10-110000-00-00NoNoCurrent
63629-8890-36362988900390 TABLET in 1 BOTTLE (63629-8890-3) 90 tablet2021-10-110000-00-00NoNoCurrent
63629-8890-463629889004120 TABLET in 1 BOTTLE (63629-8890-4) 120 tablet2021-10-110000-00-00NoNoCurrent