Pantoprazole Sodium
- Product NDC
- 68788-7545
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202038
- Marketing category
- ANDA
- Substance
- PANTOPRAZOLE SODIUM
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-7545-1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-1) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7545-3 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-3) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7545-6 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-6) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7545-8 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-8) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7545-9 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-9) | 2019-12-27 | 0000-00-00 | No | Current |