NDC codes

FDA NDC Directory
Product NDC (as listed)72189-632Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0632Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
72189-632-30721890632307218906323030 TABLET in 1 BOTTLE (72189-632-30)Marketed from Jul 22, 2025
72189-632-60721890632607218906326060 TABLET in 1 BOTTLE (72189-632-60)Marketed from Jul 22, 2025
72189-632-90721890632907218906329090 TABLET in 1 BOTTLE (72189-632-90)Marketed from Jul 22, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Oxycodone HCL
Generic name (nonproprietary)
oxycodone hcl
Active ingredients
Oxycodone hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_RxNDC labeler code 72189
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077712
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 72189-632_3a8579d0-8ea3-42bc-e063-6294a90a7fd2SPL ID 3a8579d0-8ea3-42bc-e063-6294a90a7fd2SPL set ID 3a849aeb-b72c-5cde-e063-6394a90a9768RxCUI 1049683UNII C1ENJ2TE6C
Pharmacologic class
Opioid Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472189063230 followed by a unit qualifier and the quantity

Package 72189-0632-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Oxycodone hydrochloride is indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration [see Warnings and Precautions (5.1)], reserve oxycodone hydrochloride for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products): Have not been tolerated or are not expected to be tolerated, Have not provided adequate analgesia or are not expected to provide adequate analgesia. Oxycodone hydrochloride should not be used for an extended period of t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-632

What is NDC 72189-632?
72189-632 is the product NDC for Oxycodone HCL, Oxycodone hydrochloride 10 mg/1 tablet, listed with the FDA by Direct_Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxycodone HCL.
What is the active ingredient?
Oxycodone hydrochloride.
Who is the labeler?
Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxycodone HCL?
4 other product NDCs are listed under this name. See all Oxycodone HCL NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Oxycodone HCL NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Oxycodone HCLOxycodone hydrochloride 5 mg/1TabletOralDirect_Rx72189-61872189-0618-3072189-0618-60
Oxycodone HCLOxycodone hydrochloride 20 mg/1TabletOralDirect_Rx72189-61372189-0613-30
Oxycodone HCLOxycodone hydrochloride 15 mg/1TabletOralDirect_Rx72189-61472189-0614-3072189-0614-6072189-0614-90
Oxycodone HCLOxycodone hydrochloride 5 mg/1TabletOralDirect_Rx72189-61172189-0611-30

Other NDCs under ANDA 077712

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 077712
ProductStrengthForm · routeLabelerProduct NDC
Oxycodone HCLOxycodone hydrochloride 20 mg/1TabletOralDirect_Rx72189-613
Oxycodone HCLOxycodone hydrochloride 15 mg/1TabletOralDirect_Rx72189-614
Oxycodone HCLOxycodone hydrochloride 5 mg/1TabletOralDirect_Rx72189-618
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-956
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralStrides Pharma Science Limited64380-259
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralStrides Pharma Science Limited64380-260
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralStrides Pharma Science Limited64380-261
Oxycodone HydrochlorideOxycodone hydrochloride 20 mg/1TabletOralStrides Pharma Science Limited64380-262
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralStrides Pharma Science Limited64380-263
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralRedpharm Drug67296-2188
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack71335-2816
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralAsclemed USA, Inc.76420-362
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralAsclemed USA, Inc.76420-363
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralAsclemed USA, Inc.76420-364
Oxycodone HydrochlorideOxycodone hydrochloride 20 mg/1TabletOralAsclemed USA, Inc.76420-365
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralAsclemed USA, Inc.76420-366

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