Pantoprazole Sodium
- Product NDC
- 58118-1429
- 11-digit product format
- 581181429
- Labeler code
- 58118
- Product ID
- 58118-1429_8d7eb983-7507-3f2f-e053-2995a90a9ea3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA090074
- Marketing category
- ANDA
- Marketing start
- 2018-01-17
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-1429 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [CLINICAL SOLUTIONS WHOLESALE, LLC] | 3 | Legacy NDC | 20190713_9cbd7d6a-c69f-469c-9f87-cb2db9260f25.zip |