PANTOPRAZOLE SODIUM
- Product NDC
- 50742-151
- 11-digit product format
- 507420151
- Labeler code
- 50742
- Product ID
- 50742-151_11f2b84d-472b-40de-aff3-9d476bcf7b22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pantoprazole sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA211368
- Marketing category
- ANDA
- Marketing start
- 2019-03-11
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-151-10 | 50742015110 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (50742-151-10) | 2019-03-11 | 0000-00-00 | No | No | Current |
| 50742-151-90 | 50742015190 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50742-151-90) | 2019-03-11 | 0000-00-00 | No | No | Current |