Pantoprazole Sodium
- Product NDC
- 58118-0617
- 11-digit product format
- 581180617
- Labeler code
- 58118
- Product ID
- 58118-0617_ae6a6224-67a1-04d4-e053-2a95a90af047
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0617-8 | 58118061708 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58118-0617-8) | 2020-04-09 | 0000-00-00 | No | No | Current |