Probenecid is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Marlex Pharmaceuticals Inc. The primary component is Probenecid.
| Product ID | 10135-541_3c246752-b856-470e-80c2-34731d535cec |
| NDC | 10135-541 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Probenecid |
| Generic Name | Probenecid |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1976-07-29 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA080966 |
| Labeler Name | Marlex Pharmaceuticals Inc |
| Substance Name | PROBENECID |
| Active Ingredient Strength | 500 mg/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 1976-07-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA080966 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1976-07-29 |
| Marketing Category | ANDA |
| Application Number | ANDA080966 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1976-07-29 |
| Ingredient | Strength |
|---|---|
| PROBENECID | 500 mg/1 |
| SPL SET ID: | 5d552de5-2d18-4464-bcaf-0311fa3f080d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0378-0156 | Probenecid | probenecid |
| 0527-1367 | Probenecid | Probenecid |
| 0591-5347 | Probenecid | Probenecid |
| 10135-541 | Probenecid | Probenecid |
| 11819-282 | Probenecid | Probenecid |
| 43353-839 | Probenecid | Probenecid |
| 43353-991 | Probenecid | probenecid |
| 63629-8213 | Probenecid | Probenecid |
| 68084-945 | Probenecid | Probenecid |
| 68151-1993 | Probenecid | probenecid |
| 69367-154 | Probenecid | Probenecid |
| 71335-1697 | Probenecid | Probenecid |
| 71626-999 | Probenecid | Probenecid |