Pantoprazole Sodium
- Product NDC
- 63629-8112
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202038
- Marketing category
- ANDA
- Substance
- PANTOPRAZOLE SODIUM
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 63629-8112-1 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-8112-1) | 2019-07-18 | 0000-00-00 | No | Current |