NDC codes

FDA NDC Directory
Product NDC (as listed)60760-966Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0966Add 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
60760-966-30607600966306076009663030 TABLET in 1 BOTTLE, PLASTIC (60760-966-30)Marketed from Jul 24, 2026
60760-966-60607600966606076009666060 TABLET in 1 BOTTLE, PLASTIC (60760-966-60)Marketed from Jul 24, 2026

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 Hydrochloride
Generic name (nonproprietary)
oxycodone hydrochloride
Active ingredients
Oxycodone hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207418
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 60760-966_57afede2-23b4-c9e6-e063-6394a90abd35SPL ID 57afede2-23b4-c9e6-e063-6394a90abd35SPL set ID 57afed61-79db-ca43-e063-6394a90a68ebRxCUI 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

N460760096630 followed by a unit qualifier and the quantity

Package 60760-0966-30. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 60760-966

What is NDC 60760-966?
60760-966 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 10 mg/1 tablet, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxycodone Hydrochloride.
What is the active ingredient?
Oxycodone hydrochloride.
Who is the labeler?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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 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
Oxycodone HydrochlorideOxycodone hydrochloride 20 mg/1TabletOralStrides Pharma Science Limited64380-26264380-0262-01

All 131 Oxycodone Hydrochloride NDCs

Other NDCs under ANDA 207418

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

FDA NDC Directory listings under ANDA 207418
ProductStrengthForm · routeLabelerProduct NDC
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack63629-1930
Oxycodone HydrochlorideOxycodone hydrochloride 10 mg/1TabletOralCamber Pharmaceuticals Inc31722-485
Oxycodone HydrochlorideOxycodone hydrochloride 20 mg/1TabletOralCamber Pharmaceuticals Inc31722-486
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-967
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralXLCare Pharmaceuticals, Inc72865-128
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralXLCare Pharmaceuticals, Inc72865-129
Oxycodone HydrochlorideOxycodone hydrochloride 15 mg/1TabletOralCamber Pharmaceuticals Inc31722-917
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralCamber Pharmaceuticals Inc31722-918
Oxycodone HydrochlorideOxycodone hydrochloride 5 mg/1TabletOralCamber Pharmaceuticals Inc31722-484
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack63629-8890
Oxycodone HydrochlorideOxycodone hydrochloride 30 mg/1TabletOralBryant Ranch Prepack71335-2126

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