Pantoprazole Sodium
- Product NDC
- 60760-646
- 11-digit product format
- 607600646
- Labeler code
- 60760
- Product ID
- 60760-646_e8815323-26a9-4f59-e053-2995a90ab690
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2022-08-25
- 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 |
|---|
| 60760-646 | PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20220914_e8816b1f-2f29-b26e-e053-2a95a90a92f3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-646-30 | 60760064630 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30) | 2022-08-25 | 0000-00-00 | No | No | Current |