Oxycodone Hydrochloride NDC 10702-171

NDC codes

FDA NDC Directory

Product NDC (as listed)10702-171Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10702-0171Add 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
10702-171-03	10702017103	1 BOTTLE, PLASTIC in 1 CARTON (10702-171-03) / 30 mL in 1 BOTTLE, PLASTICMarketed from Jul 21, 2017

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 — 100 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: KVK-Tech, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208593
Marketing start: Jul 21, 2017
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 10702-171_57c47d8d-7920-cd93-e063-6294a90a737aSPL ID 57c47d8d-7920-cd93-e063-6294a90a737aSPL set ID 744f5d1c-7427-492c-8994-c8e817793e53RxCUI 1049604, 1049615UNII 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

N410702017103 followed by a unit qualifier and the quantity

Package 10702-0171-03. 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 Jul 29, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Oxycodone Hydrochloride Oral Solution is indicated in adults for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Oxycodone Hydrochloride Oral Solution 100 mg per 5 mL (20 mg/mL) is indicated for use in opioid-tolerant adult patients who require higher doses of opioids for the management of pain severe enough to require an opioid analgesic and for which alternate treatments are inadequate. Limitations of Use • Because of the risks of addiction, abuse, misuse, overdose, and death, which can occur at any dosage or duration, and persist over the course of therapy [see Warnings and Precautions (5.2)] , reserve opioid analges…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208593

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

FDA NDC Directory listings under ANDA 208593
Product	Strength	Form · route	Labeler	Product NDC
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/5mL	SolutionOral	KVK-Tech, Inc.	10702-183