Pantoprazole sodium delayed-release
- Product NDC
- 70756-019
- 11-digit product format
- 707560019
- Labeler code
- 70756
- Product ID
- 70756-019_2c507c43-c033-4b6e-b954-f0f2fb617289
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole sodium delayed-release
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lifestar Pharma LLC
- Application
- ANDA215880
- Marketing category
- ANDA
- Marketing start
- 2022-07-27
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70756-019-12 | Pantoprazole sodium delayed-release | 1000 in 1 BOTTLE | TABLET | 1000 | | 11 |
| 70756-019-90 | Pantoprazole sodium delayed-release | 90 in 1 BOTTLE | TABLET | 90 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70756-019 | PANTOPRAZOLE SODIUM DELAYED-RELEASE TABLET [LIFESTAR PHARMA LLC] | 10 | Current NDC, Legacy NDC, 2 package rows | 20240503_0502f935-af7a-4f1e-8c3e-29e20647c885.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70756-019-12 | 70756001912 | 1000 TABLET in 1 BOTTLE (70756-019-12) | 1000 tablet | 2022-07-27 | 0000-00-00 | No | No | Current |
| 70756-019-90 | 70756001990 | 90 TABLET in 1 BOTTLE (70756-019-90) | 90 tablet | 2022-07-27 | 0000-00-00 | No | No | Current |