Prescription drug · ANDA
Etodolac NDC 70518-4291
Etodolac 500 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4291-0 | 70518429100 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4291-0)Marketed from Feb 25, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Etodolac
- Generic name (nonproprietary)
- etodolac
- Active ingredients
- Etodolac — 500 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075074
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 70518-4291_5a966262-e673-f96e-e063-6294a90aef2cSPL ID 5a966262-e673-f96e-e063-6294a90aef2cSPL set ID 188cdd2e-4196-458c-9631-4fa9a0d309b8RxCUI 199390UNII 2M36281008
- 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
N470518429100followed by a unit qualifier and the quantityPackage 70518-4291-00. 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 etodolac capsules and tablets and other treatment options before deciding to use etodolac capsules and tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Etodolac Capsules and Tablets are indicated: For acute and long-term use in the management of signs and symptoms of the following: Osteoarthritis Rheumatoid arthritis For the management of acute pain
Excerpt only. Read the full label for complete information.
About NDC 70518-4291
- What is NDC 70518-4291?
- 70518-4291 is the product NDC for Etodolac, Etodolac 500 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. 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?
- REMEDYREPACK INC., NDC labeler code 70518. 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 400 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-461 | 59651-0461-01 |
| 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 |
Other NDCs under ANDA 075074
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 |
|---|---|---|---|---|
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8673 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1958 |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-1489 |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-779 |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-795 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Advanced Rx of Tennessee, LLC | 80425-0551 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-816 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Golden State Medical Supply, Inc. | 60429-311 |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | Golden State Medical Supply, Inc. | 60429-312 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-859 |
| Etodolac | Etodolac 400 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4018 |
| Etodolac | Etodolac 500 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4036 |