OXYCODONE HYDROCHLORIDE

Product NDC
55700-175
11-digit product format
557000175
Labeler code
55700
Product ID
55700-175_1359d9b6-085e-4c79-b421-d4339ed08b5a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
OXYCODONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA091393
Marketing category
ANDA
Marketing start
2013-10-18
Marketing end
0000-00-00
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
2020-12-31
Current FDA listing
Historical FDA.report record

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
55700-175-01OXYCODONE HYDROCHLORIDE120 in 1 BOTTLETABLET1209
55700-175-30OXYCODONE HYDROCHLORIDE30 in 1 BOTTLETABLET309
55700-175-60OXYCODONE HYDROCHLORIDE60 in 1 BOTTLETABLET609
55700-175-90OXYCODONE HYDROCHLORIDE90 in 1 BOTTLETABLET909

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-175-01EA - Each55700-175a0afc2ce-c29f-4d5c-877d-c0d298421fb312015-12-02
55700-175-30EA - Each55700-1751b51fd09-3076-48b2-8b00-0df06de17af912015-12-02
55700-175-60EA - Each55700-1755887feb2-d3de-46ed-a392-4c4e4ae2ff2e12015-12-02
55700-175-90EA - Each55700-17502c592d6-f544-4d92-b935-ea5617c55bdb12015-12-02

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55700-175OXYCODONE HYDROCHLORIDE TABLET [QUALITY CARE PRODUCTS LLC]9Legacy NDC, 4 package rows20241222_4cadb809-157d-49cc-97b4-3276594f19d2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049611oxyCODONE HCl 15 MG Oral TabletPSN4cadb809-157d-49cc-97b4-3276594f19d29
1049618oxyCODONE HCl 30 MG Oral TabletPSN4cadb809-157d-49cc-97b4-3276594f19d29
1049611oxycodone hydrochloride 15 MG Oral TabletSCD4cadb809-157d-49cc-97b4-3276594f19d29
1049618oxycodone hydrochloride 30 MG Oral TabletSCD4cadb809-157d-49cc-97b4-3276594f19d29

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-175-0155700017501120 TABLET in 1 BOTTLE (55700-175-01) 120 tablet2013-10-180000-00-00NoNoCurrent
55700-175-305570001753030 TABLET in 1 BOTTLE (55700-175-30) 30 tablet2013-10-180000-00-00NoNoCurrent
55700-175-605570001756060 TABLET in 1 BOTTLE (55700-175-60) 60 tablet2013-10-180000-00-00NoNoCurrent
55700-175-905570001759090 TABLET in 1 BOTTLE (55700-175-90) 90 tablet2013-10-180000-00-00NoNoCurrent