Pantoprazole Sodium
- Product NDC
- 68071-2231
- 11-digit product format
- 680712231
- Labeler code
- 68071
- Product ID
- 68071-2231_ac397028-d91c-5089-e053-2a95a90ac0c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090074
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6871619Q5X | PANTOPRAZOLE SODIUM | 164579-32-2 | PANTOPRAZOLE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2231-3 | 68071223103 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2231-3) | 2020-08-06 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pantoprazole Sodium | NuCare Pharmaceuticals,Inc. | 2020-08-06 | HUMAN PRESCRIPTION DRUG LABEL | 1 |