Drug for further processing · DRUG FOR FURTHER PROCESSING
Etodolac NDC 59651-461
Etodolac 400 mg/1 · Tablet, Film coated · Aurobindo Pharma Limited
Unfinished product
This listing is a drug for further processing, not a finished drug product dispensed or administered to patients. It is not normally billed.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59651-461-07 | 59651046107 | 1600 TABLET, FILM COATED in 1 BAG (59651-461-07)Marketed from 15-JUL-26 |
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
- Generic name (nonproprietary)
- etodolac
- Active ingredients
- Etodolac — 400 mg/1
- Dosage form
- Tablet, Film coated
- Labeler
- Aurobindo Pharma LimitedNDC labeler code 59651
- Product type
- Drug for further processing
- Marketing category
- Drug for further processing
- Marketing start
- Listing expires
- Identifiers
- Product ID 59651-461_f8a9c3c6-0293-4e0c-883c-93d8397a9e6cSPL ID f8a9c3c6-0293-4e0c-883c-93d8397a9e6c
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N459651046107followed by a unit qualifier and the quantityPackage 59651-0461-07. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 59651-461
- What is NDC 59651-461?
- 59651-461 is the product NDC for Etodolac, Etodolac 400 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Etodolac.
- What is the active ingredient?
- Etodolac.
- Who is the labeler?
- Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Etodolac?
- 100 other product NDCs are listed under this name. See all Etodolac NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Etodolac products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-462 | 59651-0462-01 |
| etodolac | Etodolac 400 mg/1 | TabletOral | Ipca Laboratories Limited | 83980-029 | 83980-0029-0183980-0029-1083980-0029-13 |
| etodolac | Etodolac 500 mg/1 | TabletOral | Ipca Laboratories Limited | 83980-030 | 83980-0030-0183980-0030-0583980-0030-13 |
| etodolac | Etodolac 200 mg/1 | CapsuleOral | Ipca Laboratories Limited | 83980-031 | 83980-0031-0183980-0031-0583980-0031-13 |
| etodolac | Etodolac 300 mg/1 | CapsuleOral | Ipca Laboratories Limited | 83980-032 | 83980-0032-0183980-0032-0583980-0032-13 |
| etodolac | Etodolac 300 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-8037 | 50090-8037-01 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4542 | 70518-4542-00 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Advanced Rx of Tennessee, LLC | 80425-0551 | 80425-0551-01 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8846 | 68788-8846-0168788-8846-0268788-8846-03+2 more |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4291 | 70518-4291-00 |