PANTOPRAZOLE SODIUM
- Product NDC
- 70518-2494
- 11-digit product format
- 705182494
- Labeler code
- 70518
- Product ID
- 70518-2494_c9b11581-e194-297e-e053-2a95a90a3fad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2019-12-18
- 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
- 2022-12-31
- 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 |
|---|
| 70518-2494-0 | 70518249400 | 28 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2494-0) | 2019-12-18 | 0000-00-00 | No | No | Current |
| 70518-2494-1 | 70518249401 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2494-1) | 2020-01-22 | 0000-00-00 | No | No | Current |