Pantoprazole sodium
- Product NDC
- 70095-024
- 11-digit product format
- 700950024
- Labeler code
- 70095
- Product ID
- 70095-024_b423abbc-01e1-4d07-9c89-a7398c898d2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole sodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sun Pharmaceutical Industries Limited
- Application
- ANDA204400
- Marketing category
- ANDA
- Marketing start
- 2023-04-03
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 mg/10mL
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70095-024-02 | 70095002402 | 10 CARTON in 1 PACKAGE (70095-024-02) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) | 10 carton | 2023-04-03 | No | No | Historical |
| 70095-024-03 | 70095002403 | 25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) | 25 carton | 2023-04-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pantoprazole sodium | Sun Pharmaceutical Industries Limited | Gland Pharma Limited | 2025-04-01 | Human Prescription Drug Label | 4 |