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Probenecid
Probenecid - 11819-282-08 - (Probenecid)
Drug Information of Probenecid
| Product NDC: | 11819-282 |
| Proprietary Name: | Probenecid |
| Non Proprietary Name: | Probenecid |
| Active Ingredient(s): | 500 mg/1 & nbsp; Probenecid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Probenecid
| Product NDC: | 11819-282 |
| Labeler Name: | HHS/Program Support Center/Supply Service Center |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084442 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830701 |
Package Information of Probenecid
| Package NDC: | 11819-282-08 |
| Package Description: | 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11819-282-08) |
NDC Information of Probenecid
| NDC Code | 11819-282-08 |
| Proprietary Name | Probenecid |
| Package Description | 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11819-282-08) |
| Product NDC | 11819-282 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Probenecid |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19830701 |
| Marketing Category Name | ANDA |
| Labeler Name | HHS/Program Support Center/Supply Service Center |
| Substance Name | PROBENECID |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
