Probenecid
- Product NDC
- 71335-1697
- 11-digit product format
- 713351697
- Labeler code
- 71335
- Product ID
- 71335-1697_ab121e7d-8c54-417d-a657-a8b82741b9b0
- 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
- Marketing end
- 0000-00-00
- Substance
- PROBENECID
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-1697-1 | Probenecid | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1697 | PROBENECID TABLET, FILM COATED [BRYANT RANCH PREPACK] | 2 | Legacy NDC, 1 package rows | 20220204_ab121e7d-8c54-417d-a657-a8b82741b9b0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1697-1 | 71335169701 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1697-1) | 2020-08-26 | 0000-00-00 | No | No | Current |