Pantoprazole Sodium
- Product NDC
- 72603-746
- 11-digit product format
- 726030746
- Labeler code
- 72603
- Product ID
- 72603-746_6637d90b-b268-4a5f-ab5b-885f2d5f0d4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2026-03-01
- 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
- 2027-12-31
- 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 |
|---|
| 72603-746-01 | 72603074601 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-746-01) | 2026-03-01 | No | No | Historical |
| 72603-746-02 | 72603074602 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-746-02) | 2026-03-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pantoprazole Sodium | NorthStar Rx LLC | Aurobindo Pharma Limited | 2026-02-06 | Human Prescription Drug Label | 1 |