NDC 71626-999
Probenecid
Probenecid
Probenecid is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Medstone Pharma Llc. The primary component is Probenecid.
| Product ID | 71626-999_0ffb25c6-72a5-4aa2-a389-1e57f0eb06de |
| NDC | 71626-999 |
| 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 | Medstone Pharma LLC |
| Substance Name | PROBENECID |
| Active Ingredient Strength | 500 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |