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NDC 50090-2133-00 Etodolac 500 mg/1 Details
Etodolac 500 mg/1
Etodolac is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is ETODOLAC.
MedlinePlus Drug Summary
Etodolac tablets, capsules, and extended-release (long-acting) tablets are used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Etodolac tablets and capsules are also used to relieve pain from other causes. Etodolac is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
Related Packages: 50090-2133-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Etodolac
Product Information
| NDC | 50090-2133 |
|---|---|
| Product ID | 50090-2133_db7bc3b1-762a-4722-93af-4f313a7e2d35 |
| Associated GPIs | 66100008000320 |
| GCN Sequence Number | 027368 |
| GCN Sequence Number Description | etodolac TABLET 500 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 61766 |
| HICL Sequence Number | 006089 |
| HICL Sequence Number Description | ETODOLAC |
| Brand/Generic | Generic |
| Proprietary Name | Etodolac |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Etodolac |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | ETODOLAC |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076004 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-2133-00 (50090213300)
| NDC Package Code | 50090-2133-0 |
|---|---|
| Billing NDC | 50090213300 |
| Package | 20 TABLET, FILM COATED in 1 BOTTLE (50090-2133-0) |
| Marketing Start Date | 2015-10-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |