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NDC 72789-0040-30 Nabumetone 750 mg/1 Details
Nabumetone 750 mg/1
Nabumetone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. 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: 72789-0040-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Nabumetone
Product Information
NDC | 72789-0040 |
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Product ID | 72789-040_fe4577fa-39e3-ccad-e053-6294a90a9ee4 |
Associated GPIs | 66100055000330 |
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 |
Route | ORAL |
Active Ingredient Strength | 750 |
Active Ingredient Units | mg/1 |
Substance Name | NABUMETONE |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
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 | ANDA078420 |
Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0040-30 (72789004030)
NDC Package Code | 72789-040-30 |
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Billing NDC | 72789004030 |
Package | 30 TABLET in 1 BOTTLE, PLASTIC (72789-040-30) |
Marketing Start Date | 2019-12-17 |
NDC Exclude Flag | N |
Pricing Information | N/A |