Probenecid
- Product NDC
- 71626-999
- 11-digit product format
- 716260999
- Labeler code
- 71626
- Product ID
- 71626-999_4f994162-c2e7-4c39-95dd-d9d16ebde294
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Probenecid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Medstone Pharma LLC
- 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
- 2022-12-31
- 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 |
|---|
| 71626-999-08 | Probenecid | 8 in 1 BOTTLE | TABLET, FILM COATED | 8 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71626-999 | PROBENECID TABLET, FILM COATED [MEDSTONE PHARMA LLC] | 2 | Legacy NDC, 1 package rows | 20210213_69637b68-8ee2-49ac-9393-e17b01041ea7.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 |
|---|
| 71626-999-08 | 71626099908 | 8 TABLET, FILM COATED in 1 BOTTLE (71626-999-08) | 2020-09-04 | 0000-00-00 | No | No | Current |