PANTOPRAZOLE SODIUM
- Product NDC
- 68645-596
- 11-digit product format
- 686450596
- Labeler code
- 68645
- Product ID
- 68645-596_e7b92b59-2448-5bc1-e053-2995a90aa7b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2014-09-10
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-596 | PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 14 | Legacy NDC | 20241109_de0f3767-9dba-4de7-e053-2a95a90aa3c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-596-54 | 68645059654 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68645-596-54) | 2014-09-10 | 0000-00-00 | No | No | Current |