Search by Drug Name or NDC
NDC 16571-0688-09 FENOPROFEN CALCIUM 400 mg/1 Details
FENOPROFEN CALCIUM 400 mg/1
FENOPROFEN CALCIUM is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is FENOPROFEN CALCIUM.
MedlinePlus Drug Summary
Fenoprofen 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). Fenoprofen is also used to relieve mild to moderate pain from other causes. Fenoprofen 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: 16571-0688-09Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fenoprofen
Product Information
| NDC | 16571-0688 |
|---|---|
| Product ID | 16571-688_b3a58d34-7780-4056-b144-bad674c51494 |
| Associated GPIs | |
| GCN Sequence Number | 065880 |
| GCN Sequence Number Description | fenoprofen calcium CAPSULE 400 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 27999 |
| HICL Sequence Number | 003724 |
| HICL Sequence Number Description | FENOPROFEN CALCIUM |
| Brand/Generic | Generic |
| Proprietary Name | FENOPROFEN CALCIUM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | FENOPROFEN CALCIUM |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 400 |
| Active Ingredient Units | mg/1 |
| Substance Name | FENOPROFEN CALCIUM |
| Labeler Name | Rising Pharma Holdings, 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 | ANDA214475 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 16571-0688-09 (16571068809)
| NDC Package Code | 16571-688-09 |
|---|---|
| Billing NDC | 16571068809 |
| Package | 90 CAPSULE in 1 BOTTLE (16571-688-09) |
| Marketing Start Date | 2022-08-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |