NDC codes

FDA NDC Directory
Product NDC (as listed)43602-190Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43602-0190Add 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
43602-190-31436020190314360201903130 mL in 1 BOTTLE (43602-190-31)Marketed from Jul 13, 2017
43602-190-504360201905043602019050500 mL in 1 BOTTLE (43602-190-50)Marketed from Jul 13, 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 — 5 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Ascent Pharmaceuticals IncNDC labeler code 43602
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209021
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 43602-190_46183e47-ba04-4b02-912a-6aeed41c609eSPL ID 46183e47-ba04-4b02-912a-6aeed41c609eSPL set ID de96e2be-66d9-4bcb-a133-221ad32e09f1RxCUI 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

N443602019031 followed by a unit qualifier and the quantity

Package 43602-0190-31. 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 Oral Solution is 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, and misuse with opioids, even at recommended doses, [see Warnings and Precautions (5.2)] , reserve Oxycodone Hydrochloride Oral Solution for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products]: Have not been tolerated, or are not expected to be tolerated, Have not provided adequate analgesia, or are not expected to provide adequate analgesia Oxycodone Hydrochloride Oral Solution is an opioid agon…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43602-190

What is NDC 43602-190?
43602-190 is the product NDC for Oxycodone Hydrochloride, Oxycodone hydrochloride 5 mg/5mL solution, listed with the FDA by Ascent Pharmaceuticals 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?
Ascent Pharmaceuticals Inc, NDC labeler code 43602. 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 209021

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

FDA NDC Directory listings under ANDA 209021
ProductStrengthForm · routeLabelerProduct NDC
Oxycodone HydrochlorideOxycodone hydrochloride 100 mg/5mLSolutionOralAscent Pharmaceuticals Inc43602-198

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