PANTOPRAZOLE SODIUM
- Product NDC
- 68788-7798
- 11-digit product format
- 687887798
- Labeler code
- 68788
- Product ID
- 68788-7798_a4683a93-8bd5-4877-8fd4-0615ab3d60f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2014-09-10
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 20 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 |
|---|
| 68788-7798 | PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [PREFERRED PHARMACEUTICALS, INC.] | 5 | Legacy NDC | 20240727_f1637b9b-67b3-43dd-8d46-6cae5f582bec.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7798-1 | 68788779801 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-1) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7798-3 | 68788779803 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-3) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7798-6 | 68788779806 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-6) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7798-8 | 68788779808 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-8) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7798-9 | 68788779809 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7798-9) | 2020-10-13 | 0000-00-00 | No | No | Current |