PANTOPRAZOLE SODIUM
- Product NDC
- 55700-850
- 11-digit product format
- 557000850
- Labeler code
- 55700
- Product ID
- 55700-850_ce8cb1a4-2ced-47b0-b0a6-0d2f103b3f15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA202882
- Marketing category
- ANDA
- Marketing start
- 2020-03-20
- 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 |
|---|
| 55700-850 | PANTOPRAZOLE SODIUM (PANTOPRAZOLE) TABLET, DELAYED RELEASE [QUALITY CARE PRODUCTS, LLC] | 11 | Legacy NDC | 20241220_65098903-ccb5-4daf-ab1b-d9823fc73066.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-850-30 | 55700085030 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-30) | 2020-03-20 | 0000-00-00 | No | No | Current |
| 55700-850-60 | 55700085060 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-60) | 2020-03-20 | 0000-00-00 | No | No | Current |
| 55700-850-90 | 55700085090 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-90) | 2020-03-20 | 0000-00-00 | No | No | Current |