Probenecid
- Product NDC
- 72162-2237
- 11-digit product format
- 721622237
- Labeler code
- 72162
- Product ID
- 72162-2237_8c261b93-98b4-46ce-a713-11d3b2d7cd13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Probenecid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080966
- Marketing category
- ANDA
- Marketing start
- 1976-07-29
- Substance
- PROBENECID
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| PO572Z7917 | PROBENECID | 57-66-9 | PROBENECID |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2237-1 | 72162223701 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1) | 2024-01-26 | No | No | Historical |