NDC codes

FDA NDC Directory
Product NDC (as listed)0904-7180Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-7180Add 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
0904-7180-610090471806100904718061100 BLISTER PACK in 1 CARTON (0904-7180-61) / 1 TABLET in 1 BLISTER PACKMarketed from Oct 30, 2012

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
Active ingredients
Oxycodone hydrochloride — 15 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Major PharmaceuticalsNDC labeler code 0904
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 0904-7180_cf18b924-ef1c-4b84-9c6d-6977ee8b7407SPL ID cf18b924-ef1c-4b84-9c6d-6977ee8b7407SPL set ID 6b6db42b-9821-4aa6-8566-297037d84079RxCUI 1049611, 1049621UNII 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

N400904718061 followed by a unit qualifier and the quantity

Package 00904-7180-61. 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, 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 HCl 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 HCl tablets are an opioid agonist indicated for the management of pain severe…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0904-7180

What is NDC 0904-7180?
0904-7180 is the product NDC for Oxycodone Hydrochloride (oxycodone), Oxycodone hydrochloride 15 mg/1 tablet, listed with the FDA by Major Pharmaceuticals. It has 1 package NDC, 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?
Major Pharmaceuticals, NDC labeler code 0904. 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 5 mg/1TabletOralRedpharm Drug67296-2233
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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