Pantoprazole Sodium
- Product NDC
- 68788-9419
- 11-digit product format
- 687889419
- Labeler code
- 68788
- Product ID
- 68788-9419_e4d3a949-07ad-4214-b344-122c3f3fd48d
- 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
- 2011-01-20
- 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
- 2021-12-31
- 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 |
|---|
| 68788-9419-1 | 68788941901 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-9419-1) | 2011-01-20 | 0000-00-00 | No | No | Current |
| 68788-9419-3 | 68788941903 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-9419-3) | 2011-01-20 | 0000-00-00 | No | No | Current |
| 68788-9419-6 | 68788941906 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-9419-6) | 2011-01-20 | 0000-00-00 | No | No | Current |
| 68788-9419-8 | 68788941908 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-9419-8) | 2011-01-20 | 0000-00-00 | No | No | Current |
| 68788-9419-9 | 68788941909 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-9419-9) | 2011-01-20 | 0000-00-00 | No | No | Current |