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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Probenecid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROBENECID | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | PO572Z7917 |
| Rxcui | 198152 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2386-1 | Probenecid | 100 in 1 CONTAINER | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2386 | PROBENECID TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240816_a4f4b3e1-44a9-4b3a-9f7f-f9749ed451ca.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |