PANTOPRAZOLE SODIUM
- Product NDC
- 70518-2836
- 11-digit product format
- 705182836
- Labeler code
- 70518
- Product ID
- 70518-2836_d76f98ad-b59f-7346-e053-2995a90a64e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2020-08-18
- 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 |
|---|
| 70518-2836-0 | 70518283600 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2836-0) | 2020-08-18 | 0000-00-00 | No | No | Current |