Oxycodone Hydrochloride NDC 0406-0552

NDC codes

FDA NDC Directory

Product NDC (as listed)0406-0552Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00406-0552Add 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
0406-0552-01	00406055201	100 TABLET in 1 BOTTLE (0406-0552-01)Marketed from Jun 30, 2004
0406-0552-23	00406055223	1 TABLET in 1 BLISTER PACK (0406-0552-23)Marketed from Jun 30, 2004
0406-0552-62	00406055262	100 TABLET in 1 BLISTER PACK (0406-0552-62)Marketed from Jun 30, 2004

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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: Tablet
Route: Oral
Labeler: SpecGx LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076758
Marketing start: Jun 30, 2004
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 0406-0552_2b25e4bc-e02b-4fd0-a214-1da1b3fb5dd1SPL ID 2b25e4bc-e02b-4fd0-a214-1da1b3fb5dd1SPL set ID 928227bf-89c5-4c64-9823-0e84cc669388RxCUI 1049611, 1049618, 1049621, 1049683, 1049686UNII 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

N400406055201 followed by a unit qualifier and the quantity

Package 00406-0552-01. 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 Aug 7, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Oxycodone hydrochloride 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, 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 tablets 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 tablets are an opioid agonist indicated for the management…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076758

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

FDA NDC Directory listings under ANDA 076758
Product	Strength	Form · route	Labeler	Product NDC
Oxycodone Hydrochloride	Oxycodone hydrochloride 10 mg/1	TabletOral	SpecGx LLC	0406-8510
Oxycodone Hydrochloride	Oxycodone hydrochloride 15 mg/1	TabletOral	SpecGx LLC	0406-8515
Oxycodone Hydrochloride	Oxycodone hydrochloride 20 mg/1	TabletOral	SpecGx LLC	0406-8520
Oxycodone Hydrochloride	Oxycodone hydrochloride 30 mg/1	TabletOral	SpecGx LLC	0406-8530
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	RedPharm Drug, Inc.	67296-0425
Oxycodone Hydrochloride	Oxycodone hydrochloride 5 mg/1	TabletOral	Redpharm Drug	67296-0425