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NDC 50090-5386-03 Nabumetone 750 mg/1 Details
Nabumetone 750 mg/1
Nabumetone 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 NABUMETONE.
MedlinePlus Drug Summary
Nabumetone is 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). Nabumetone 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: 50090-5386-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Nabumetone
Product Information
NDC | 50090-5386 |
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Product ID | 50090-5386_e12e92fc-1d46-43f0-85b4-1d2c99bea8c3 |
Associated GPIs | |
GCN Sequence Number | 016575 |
GCN Sequence Number Description | nabumetone TABLET 750 MG ORAL |
HIC3 | S2B |
HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
GCN | 32962 |
HICL Sequence Number | 006311 |
HICL Sequence Number Description | NABUMETONE |
Brand/Generic | Generic |
Proprietary Name | Nabumetone |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Nabumetone |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 750 |
Active Ingredient Units | mg/1 |
Substance Name | NABUMETONE |
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 | ANDA078671 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50090-5386-03 (50090538603)
NDC Package Code | 50090-5386-3 |
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Billing NDC | 50090538603 |
Package | 60 TABLET, FILM COATED in 1 BOTTLE (50090-5386-3) |
Marketing Start Date | 2020-11-20 |
NDC Exclude Flag | N |
Pricing Information | N/A |