PANTOPRAZOLE SODIUM
- Product NDC
- 61919-134
- 11-digit product format
- 619190134
- Labeler code
- 61919
- Product ID
- 61919-134_94e52165-e8e5-a353-e053-2995a90ab296
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA077056
- Marketing category
- ANDA
- Marketing start
- 2017-02-21
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 20 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 |
|---|
| 61919-134-90 | PANTOPRAZOLE SODIUM | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-134 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE PANTOPRAZOLE SODIUM DR (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20191015_491102c1-f04b-4b7b-e054-00144ff8d46c.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 |
|---|
| 61919-134-90 | 61919013490 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-134-90) | 2017-02-21 | 0000-00-00 | No | No | Current |