NDC codes

FDA NDC Directory
Product NDC (as listed)72245-682Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72245-0682Add 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
72245-682-037224506820330 TABLET in 1 BOTTLE, PLASTIC (72245-682-03)Marketed from Feb 17, 2020
72245-682-1072245068210100 TABLET in 1 BOTTLE, PLASTIC (72245-682-10)Marketed from Feb 17, 2020

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)
Prolate
Generic name (nonproprietary)
oxycodone and acetaminophen
Active ingredients
Oxycodone hydrochloride — 7.5 mg/1Acetaminophen — 300 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040608
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 72245-682_522d935a-3cf8-b78a-e063-6294a90a4343SPL ID 522d935a-3cf8-b78a-e063-6294a90a4343SPL set ID 9cbbfa94-37b9-9652-e053-2995a90a736bRxCUI 1014599, 1014615, 1014632, 2279510, 2279512, 2279514UNII 362O9ITL9D, C1ENJ2TE6CUPC 0372245682106, 0372245681109, 0372245683103
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

N472245068203 followed by a unit qualifier and the quantity

Package 72245-0682-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 040608

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

FDA NDC Directory listings under ANDA 040608
ProductStrengthForm · routeLabelerProduct NDC
oxycodone and acetaminophenoxycodone and acetaminophen tabletsOxycodone hydrochloride 5 mg/1; Acetaminophen 300 mg/1TabletOralFH2 Pharma LLC72887-681
oxycodone and acetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 300 mg/1TabletOralFH2 Pharma LLC72887-193
oxycodone and acetaminophenOxycodone hydrochloride 7.5 mg/1; Acetaminophen 300 mg/1TabletOralFH2 Pharma LLC72887-682
oxycodone and acetaminophenoxycodone and acetaminophen tabletsOxycodone hydrochloride 10 mg/1; Acetaminophen 300 mg/1TabletOralFH2 Pharma LLC72887-683
Nalocetoxycodone and acetaminophenOxycodone hydrochloride 2.5 mg/1; Acetaminophen 300 mg/1TabletOralForte Bio-Pharma LLC72245-193
Prolateoxycodone and acetaminophenOxycodone hydrochloride 5 mg/1; Acetaminophen 300 mg/1TabletOralForte Bio-Pharma LLC72245-681
Prolateoxycodone and acetaminophenOxycodone hydrochloride 10 mg/1; Acetaminophen 300 mg/1TabletOralForte Bio-Pharma LLC72245-683

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