Pantoprazole Sodium
- Product NDC
- 63629-8112
- 11-digit product format
- 636298112
- Labeler code
- 63629
- Product ID
- 63629-8112_ca6acd19-f1ff-4a6b-9bb9-12a996fefd0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2012-09-28
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 63629-8112-1 | 63629811201 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-8112-1) | 2019-07-18 | 0000-00-00 | No | No | Current |