Search by Drug Name or NDC
NDC 70934-0011-30 meloxicam 15 mg/1 Details
meloxicam 15 mg/1
meloxicam is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is MELOXICAM.
MedlinePlus Drug Summary
Meloxicam 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). Meloxicam is also used to relieve the pain, tenderness, swelling, and stiffness caused by juvenile rheumatoid arthritis (a type of arthritis that affects children) in children 2 years of age and older. Meloxicam is in a class of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
Related Packages: 70934-0011-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Meloxicam
Product Information
| NDC | 70934-0011 |
|---|---|
| Product ID | 70934-011_f1eeb255-a691-4240-e053-2995a90acd2c |
| Associated GPIs | 66100052000330 |
| GCN Sequence Number | 029157 |
| GCN Sequence Number Description | meloxicam TABLET 15 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 31662 |
| HICL Sequence Number | 012181 |
| HICL Sequence Number Description | MELOXICAM |
| Brand/Generic | Generic |
| Proprietary Name | meloxicam |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | meloxicam |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 15 |
| Active Ingredient Units | mg/1 |
| Substance Name | MELOXICAM |
| Labeler Name | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
| 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 | ANDA077927 |
| Listing Certified Through | n/a |
Package
NDC 70934-0011-30 (70934001130)
| NDC Package Code | 70934-011-30 |
|---|---|
| Billing NDC | 70934001130 |
| Package | 30 TABLET in 1 BOTTLE, PLASTIC (70934-011-30) |
| Marketing Start Date | 2017-03-09 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |