Pantoprazole Sodium
- Product NDC
- 68788-7545
- 11-digit product format
- 687887545
- Labeler code
- 68788
- Product ID
- 68788-7545_037931ae-fd7b-49ab-bba5-04d258aa215b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2012-09-28
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7545-1 | 68788754501 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7545-3 | 68788754503 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7545-6 | 68788754506 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7545-8 | 68788754508 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-8) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7545-9 | 68788754509 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-7545-9) | 2019-12-27 | 0000-00-00 | No | No | Current |