Pantoprazole Sodium
- Product NDC
- 0781-3232
- 11-digit product format
- 007813232
- Labeler code
- 0781
- Product ID
- 0781-3232_1ffb2af5-8534-4507-9510-1932ffb52217
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA090296
- Marketing category
- ANDA
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-3232 | PANTOPRAZOLE SODIUM INJECTION, POWDER, FOR SOLUTION [SANDOZ INC] | 24 | Legacy NDC | 20250228_27c6ccc3-1041-402e-b3bc-fc779a27d584.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3232-95 | 00781323295 | 10 VIAL in 1 CARTON (0781-3232-95) > 10 mL in 1 VIAL (0781-3232-94) | 10 vial | 2020-03-30 | 0000-00-00 | No | No | Current |
| 0781-3232-96 | 00781323296 | 25 VIAL in 1 CARTON (0781-3232-96) > 10 mL in 1 VIAL (0781-3232-94) | 25 vial | 2021-05-01 | 0000-00-00 | No | No | Current |