Probenecid
- Product NDC
- 72162-2386
- 11-digit product format
- 721622386
- Labeler code
- 72162
- Product ID
- 72162-2386_c2638148-9137-410b-b35b-671a77b52412
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Probenecid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA217020
- Marketing category
- ANDA
- Marketing start
- 2023-11-20
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2386-1 | 72162238601 | 100 TABLET in 1 CONTAINER (72162-2386-1) | 100 tablet | 2024-08-15 | No | No | Historical |