What is NDC 10702-023?

10702-023 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 5 mg/1 capsule, listed with the FDA by KVK-TECH, INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.

KVK-TECH, INC., NDC labeler code 10702. 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?

131 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oxycodone Hydrochloride NDC 10702-023

NDC codes

FDA NDC Directory

Product NDC (as listed)10702-023Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10702-0023Add 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 NDC	11-digit (billing)	Package	Copy
10702-023-01	1070200230110702002301	100 CAPSULE in 1 BOTTLE (10702-023-01)Marketed from Aug 20, 2015
10702-023-06	1070200230610702002306	60 CAPSULE in 1 BOTTLE (10702-023-06)Marketed from Aug 20, 2015

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 — 5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: KVK-TECH, INC.NDC labeler code 10702
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202773
Marketing start: Aug 20, 2015
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 10702-023_5b12dc17-1788-b66c-e063-6394a90a8635SPL ID 5b12dc17-1788-b66c-e063-6394a90a8635SPL set ID 338b5391-e5f7-40a2-8b15-57f47cbc4813RxCUI 1049696UNII 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

N410702002301 followed by a unit qualifier and the quantity

Package 10702-0023-01. 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 Sep 9, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Oxycodone Hydrochloride Capsules are an opioid agonist indicated in adults 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, overdose, and death, which can occur at any dosage or duration, and persist over the course of therapy [see Warnings and Precautions (5.1)], reserve opioid analgesics, including Oxycodone Hydrochloride Capsules, for use in patients for whom alternative treatment options are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. Oxycodone Hydrochloride Capsules are an opioid ag…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10702-023

What is NDC 10702-023?: 10702-023 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 5 mg/1 capsule, listed with the FDA by KVK-TECH, INC.. 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?: KVK-TECH, INC., NDC labeler code 10702. 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?: 131 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-967	60760-0967-3060760-0967-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-966	60760-0966-3060760-0966-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 20 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-486	31722-0486-0131722-0486-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-484	31722-0484-0131722-0484-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	Camber Pharmaceuticals Inc	31722-485	31722-0485-0131722-0485-05
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-954	60760-0954-3060760-0954-60
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	Strides Pharma Science Limited	64380-259	64380-0259-0164380-0259-02
Oxycodone Hydrochloride	Oxycodone hydrochloride 20 mg/1	TabletOral	Strides Pharma Science Limited	64380-262	64380-0262-01
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	Strides Pharma Science Limited	64380-260	64380-0260-01
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	Strides Pharma Science Limited	64380-261	64380-0261-0164380-0261-02

All 132 Oxycodone Hydrochloride NDCs