NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2233Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2233Add 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
67296-2233-267296223302672962233024 TABLET in 1 BOTTLE (67296-2233-2)Marketed from Oct 30, 2012
67296-2233-367296223303672962233036 TABLET in 1 BOTTLE (67296-2233-3)Marketed from Oct 30, 2012
67296-2233-7672962233076729622330740 TABLET in 1 BOTTLE (67296-2233-7)Marketed from Oct 30, 2012

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Hydrochloride
Generic name (nonproprietary)
oxycodone
Active ingredients
Oxycodone hydrochloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Redpharm DrugNDC labeler code 67296
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203638
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 67296-2233_525002f7-1eab-cfdd-e063-6294a90a02c2SPL ID 525002f7-1eab-cfdd-e063-6294a90a02c2SPL set ID 525001a6-68d8-7ef7-e063-6294a90abc5fRxCUI 1049621UNII C1ENJ2TE6CUPC 0365162049107, 0365162048100, 0365162047103, 0365162051032, 0365162050035, 0365162048032, 0365162049039, 0365162050103, 0365162051100, 0365162047035
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

N467296223302 followed by a unit qualifier and the quantity

Package 67296-2233-02. 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 (HCl) tablets are 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 HCl tablets 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 HCl tablets should not be used for an extende…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67296-2233

What is NDC 67296-2233?
67296-2233 is the product NDC for Oxycodone Hydrochloride (oxycodone), Oxycodone hydrochloride 5 mg/1 tablet, listed with the FDA by Redpharm Drug. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxycodone Hydrochloride (Oxycodone).
What is the active ingredient?
Oxycodone hydrochloride.
Who is the labeler?
Redpharm Drug, NDC labeler code 67296. 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 Hydrochloride?
130 other product NDCs are listed under this name. See all Oxycodone Hydrochloride 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 Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-96760760-0967-3060760-0967-60
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-96660760-0966-3060760-0966-60
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralCamber Pharmaceuticals Inc31722-48431722-0484-0131722-0484-05
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralCamber Pharmaceuticals Inc31722-48531722-0485-0131722-0485-05
Oxycodone HydrochlorideOxycodone hydrochloride 20 mg/1TabletOralCamber Pharmaceuticals Inc31722-48631722-0486-0131722-0486-05
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-95460760-0954-3060760-0954-60
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-95660760-0956-3060760-0956-6060760-0956-90
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralStrides Pharma Science Limited64380-25964380-0259-0164380-0259-02
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralStrides Pharma Science Limited64380-26064380-0260-01
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralStrides Pharma Science Limited64380-26164380-0261-0164380-0261-02

All 131 Oxycodone Hydrochloride NDCs

Other NDCs under ANDA 203638

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

FDA NDC Directory listings under ANDA 203638
ProductStrengthForm · routeLabelerProduct NDC
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 5 mg/1TabletOralMajor Pharmaceuticals0904-6966
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 5 mg/1TabletOralBryant Ranch Prepack71335-0981
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-1023
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-1811
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack72162-1812
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 15 mg/1TabletOralMajor Pharmaceuticals0904-7180
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 20 mg/1TabletOralAmneal Pharmaceuticals LLC65162-050
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-047
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 10 mg/1TabletOralAmneal Pharmaceuticals LLC65162-048
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 15 mg/1TabletOralAmneal Pharmaceuticals LLC65162-049
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 30 mg/1TabletOralAmneal Pharmaceuticals LLC65162-051
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 15 mg/1TabletOralBryant Ranch Prepack71335-1080
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralPrecision Dose, Inc.68094-005
Oxycodone HydrochlorideoxycodoneOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack71335-0677

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