Pantoprazole Sodium
- Product NDC
- 51407-249
- 11-digit product format
- 514070249
- Labeler code
- 51407
- Product ID
- 51407-249_f1da5ce0-658c-0d6d-e053-2995a90a2719
- 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
- Marketing end
- 2023-03-31
- 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
- 0000-00-00
- 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 |
|---|
| 51407-249 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 8 | Legacy NDC | 20230926_8f292c85-5d6b-5ef1-e053-2a95a90a8818.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 |
|---|
| 51407-249-90 | 51407024990 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-249-90) | 2019-05-30 | 0000-00-00 | No | No | Current |