Pantoprazole Sodium
- Product NDC
- 63629-8113
- 11-digit product format
- 636298113
- Labeler code
- 63629
- Product ID
- 63629-8113_4208117b-debe-4522-8b36-24ec4226426e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090074
- 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
- 2023-12-31
- 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 |
|---|
| 63629-8113-1 | 63629811301 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-8113-1) | 2019-07-15 | 0000-00-00 | No | No | Current |
| 63629-8113-2 | 63629811302 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-8113-2) | 2019-07-15 | 0000-00-00 | No | No | Current |