Pantoprazole Sodium
- Product NDC
- 68788-6326
- 11-digit product format
- 687886326
- Labeler code
- 68788
- Product ID
- 68788-6326_60ad2c55-0686-4703-b649-6e9af9bc508a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090074
- Marketing category
- ANDA
- Marketing start
- 2016-10-18
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-6326 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [PREFERRED PHARMACEUTICALS INC.] | 8 | Legacy NDC | 20240730_884a780c-660f-4067-b519-e914ccd85241.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6326-1 | 68788632601 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6326-1) | 2016-10-18 | 0000-00-00 | No | No | Current |
| 68788-6326-3 | 68788632603 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6326-3) | 2016-10-18 | 0000-00-00 | No | No | Current |
| 68788-6326-6 | 68788632606 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6326-6) | 2016-10-18 | 0000-00-00 | No | No | Current |
| 68788-6326-8 | 68788632608 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6326-8) | 2016-10-18 | 0000-00-00 | No | No | Current |
| 68788-6326-9 | 68788632609 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-6326-9) | 2016-10-18 | 0000-00-00 | No | No | Current |