Pantoprazole Sodium
- Product NDC
- 70518-0226
- 11-digit product format
- 705180226
- Labeler code
- 70518
- Product ID
- 70518-0226_e0ca667d-526b-7bb6-e053-2a95a90ad889
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090074
- Marketing category
- ANDA
- Marketing start
- 2017-02-15
- 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 |
|---|
| 70518-0226-0 | 70518022600 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0226-0) | 2017-02-15 | 0000-00-00 | No | No | Current |
| 70518-0226-1 | 70518022601 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-0226-1) | 2017-11-21 | 0000-00-00 | No | No | Current |
| 70518-0226-2 | 70518022602 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0226-2) | 2018-05-11 | 0000-00-00 | No | No | Current |