Prescription drug · ANDA
Oxycodone And Acetaminophen NDC 87063-034
Oxycodone hydrochloride 10 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral · Asclemed USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87063-034-01 | 87063003401 | 100 TABLET in 1 BOTTLE (87063-034-01)Marketed from Nov 25, 2025 | |
| 87063-034-05 | 87063003405 | 500 TABLET in 1 BOTTLE (87063-034-05)Marketed from Nov 25, 2025 | |
| 87063-034-10 | 87063003410 | 10 TABLET in 1 BOTTLE (87063-034-10)Marketed from Nov 25, 2025 | |
| 87063-034-20 | 87063003420 | 20 TABLET in 1 BOTTLE (87063-034-20)Marketed from Nov 25, 2025 | |
| 87063-034-30 | 87063003430 | 30 TABLET in 1 BOTTLE (87063-034-30)Marketed from Nov 25, 2025 | |
| 87063-034-60 | 87063003460 | 60 TABLET in 1 BOTTLE (87063-034-60)Marketed from Nov 25, 2025 | |
| 87063-034-90 | 87063003490 | 90 TABLET in 1 BOTTLE (87063-034-90)Marketed from Nov 25, 2025 |
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 And Acetaminophen
- Generic name (nonproprietary)
- oxycodone and acetaminophen
- Active ingredients
- Oxycodone hydrochloride — 10 mg/1Acetaminophen — 325 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Asclemed USA, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 207510
- Marketing start
- Listing expires
- DEA schedule
- CII
- Other FDA classes
- Full Opioid Agonists (Mechanism)
- Identifiers
- Product ID 87063-034_44677216-216d-f82c-e063-6294a90a3dcaSPL ID 44677216-216d-f82c-e063-6294a90a3dcaSPL set ID e0d06ec7-9846-4e04-8660-5fd6b2b8e423RxCUI 1049214, 1049221, 1049225UNII 362O9ITL9D, 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
N487063003401followed by a unit qualifier and the quantityPackage 87063-0034-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Oxycodone and Acetaminophen Tablets, 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, which can occur at any dosage or duration [see WARNINGS ], reserve Oxycodone and Acetaminophen Tablets, for use in patients for whom alternative treatment options [e.g., non-opioid analgesics] • 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 and Acetaminophen Tablets should not be used for an extende…
Excerpt only. Read the full label for complete information.