Pantoprazole Sodium
- Product NDC
- 45865-785
- 11-digit product format
- 458650785
- Labeler code
- 45865
- Product ID
- 45865-785_7d772e48-fd28-219f-e053-2991aa0af282
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-785-30 | Pantoprazole Sodium | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-785 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20181221_7d77134c-2082-39e8-e053-2991aa0a4a3b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 45865-785-30 | 45865078530 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-785-30) | 2018-06-01 | 0000-00-00 | No | No | Current |