Probenecid
- Product NDC
- 43353-991
- 11-digit product format
- 433530991
- Labeler code
- 43353
- Product ID
- 43353-991_169cd45c-f0a8-4fe7-a1e1-e6362b5c719c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- probenecid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA084211
- Marketing category
- ANDA
- Marketing start
- 1976-01-13
- Marketing end
- 0000-00-00
- Substance
- PROBENECID
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-991-60 | 43353099160 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-991-60) | 2015-01-12 | 0000-00-00 | No | No | Current |