Prescription drug · ANDA
Nabumetone NDC 71205-030
Nabumetone 500 mg/1 · Tablet, Film coated · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-030-20 | 71205003020 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-20)Marketed from Jan 19, 2022 | |
| 71205-030-30 | 71205003030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-30)Marketed from May 1, 2018 | |
| 71205-030-60 | 71205003060 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-60)Marketed from May 1, 2018 | |
| 71205-030-90 | 71205003090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-90)Marketed from May 1, 2018 |
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)
- Nabumetone
- Generic name (nonproprietary)
- nabumetone
- Active ingredients
- Nabumetone — 500 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Proficient Rx LPNDC labeler code 71205
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 091083
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 71205-030_55d8ea63-038a-4294-9243-ca915460c1a6SPL ID 55d8ea63-038a-4294-9243-ca915460c1a6SPL set ID 0870c3c9-bfce-4722-8779-8775644196d3RxCUI 311892UNII LW0TIW155ZUPC 0371205030209
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
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
N471205003020followed by a unit qualifier and the quantityPackage 71205-0030-20. 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 Carefully consider the potential benefits and risks of nabumetone tablets and other treatment options before deciding to use nabumetone tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Nabumetone tablets are indicated for relief of signs and symptoms of osteoarthritis and rheumatoid arthritis.
Excerpt only. Read the full label for complete information.
About NDC 71205-030
- What is NDC 71205-030?
- 71205-030 is the product NDC for Nabumetone, Nabumetone 500 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Nabumetone.
- What is the active ingredient?
- Nabumetone.
- Who is the labeler?
- Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Nabumetone?
- 58 other product NDCs are listed under this name. See all Nabumetone NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Nabumetone products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Nabumetone | Nabumetone 500 mg/1 | Tablet, Film coatedOral | ANI Pharmaceuticals, Inc. | 70954-784 | 70954-0784-1070954-0784-20 |
| Nabumetone | Nabumetone 750 mg/1 | Tablet, Film coatedOral | ANI Pharmaceuticals, Inc. | 70954-785 | 70954-0785-1070954-0785-20 |
| Nabumetone | Nabumetone 750 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4047 | 70518-4047-0070518-4047-0170518-4047-02 |
| Nabumetone | Nabumetone 500 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3835 | 70518-3835-0070518-3835-01 |
| Nabumetone | Nabumetone 500 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-630 | 60687-0630-21 |
| Nabumetone | Nabumetone 750 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-733 | 51655-0733-52 |
| Nabumetone | Nabumetone 500 mg/1 | TabletOral | direct rx | 72189-184 | 72189-0184-1472189-0184-3072189-0184-60+1 more |
| Nabumetone | Nabumetone 500 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-446 | 51655-0446-2051655-0446-2551655-0446-52+1 more |
| Nabumetone | Nabumetone 500 mg/1 | TabletOral | Preferred Pharmaceuticals, Inc. | 68788-7765 | 68788-7765-0168788-7765-0268788-7765-03+3 more |
| Nabumetone | Nabumetone 500 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-396 | 51655-0396-25 |
Other NDCs under ANDA 091083
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Nabumetone | Nabumetone 500 mg/1 | Tablet, Film coatedOral | Actavis Pharma, Inc. | 0591-3670 |
| Nabumetone | Nabumetone 750 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-307 |
| Nabumetone | Nabumetone 500 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1234 |
| Nabumetone | Nabumetone 750 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1272 |