Pantoprazole Sodium
- Product NDC
- 72162-1746
- 11-digit product format
- 721621746
- Labeler code
- 72162
- Product ID
- 72162-1746_3e5421ef-0875-4a04-b17d-95cca0052c83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72162-1746-3 | 72162174603 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3) | 2024-04-04 | No | No | Historical |
| 72162-1746-6 | 72162174606 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-6) | 2024-04-04 | No | No | Historical |
| 72162-1746-9 | 72162174609 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9) | 2024-04-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pantoprazole Sodium | Bryant Ranch Prepack | 2024-04-04 | HUMAN PRESCRIPTION DRUG LABEL | 101 |