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NDC 16571-0831-10 Probenecid 500 mg/1 Details
Probenecid 500 mg/1
Probenecid is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Rising Pharma Holdings, Inc.. The primary component is PROBENECID.
MedlinePlus Drug Summary
Probenecid is used to treat chronic gout and gouty arthritis. It is used to prevent attacks related to gout, not treat them once they occur. It acts on the kidneys to help the body eliminate uric acid. Probenecid is also used to make certain antibiotics more effective by preventing the body from passing them in the urine. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 16571-0831-10Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Probenecid
Product Information
| NDC | 16571-0831 |
|---|---|
| Product ID | 16571-831_dc245b70-6a0f-4f3d-8963-a8349068ef05 |
| Associated GPIs | |
| GCN Sequence Number | 008236 |
| GCN Sequence Number Description | probenecid TABLET 500 MG ORAL |
| HIC3 | R1R |
| HIC3 Description | URICOSURIC AGENTS |
| GCN | 35072 |
| HICL Sequence Number | 003675 |
| HICL Sequence Number Description | PROBENECID |
| Brand/Generic | Generic |
| Proprietary Name | Probenecid |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Probenecid |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | PROBENECID |
| Labeler Name | Rising Pharma Holdings, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA217020 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 16571-0831-10 (16571083110)
| NDC Package Code | 16571-831-10 |
|---|---|
| Billing NDC | 16571083110 |
| Package | 1000 TABLET in 1 CONTAINER (16571-831-10) |
| Marketing Start Date | 2023-11-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |