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
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 |
|---|
| 72162-2237-1 | Probenecid | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2237 | PROBENECID TABLET, FILM COATED [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240127_6aec72b5-a9f4-45a3-82a6-7d3de64ba5e5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |