Pantoprazole Sodium
- Product NDC
- 51407-612
- 11-digit product format
- 514070612
- Labeler code
- 51407
- Product ID
- 51407-612_14d2de37-621a-5030-e063-6294a90a8632
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pantoprazole Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PANTOPRAZOLE SODIUM | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6871619Q5X |
| Rxcui | 251872, 314200 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-612-90 | Pantoprazole Sodium | 90 in 1 BOTTLE | TABLET, DELAYED RELEASE | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-612 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240331_d6aae78e-308b-7072-e053-2a95a90aaa10.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 |
|---|
| 51407-612-90 | 51407061290 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-612-90) | 2022-01-27 | 0000-00-00 | No | No | Current |