Rabeprazole Sodium
- Product NDC
- 55700-767
- 11-digit product format
- 557000767
- Labeler code
- 55700
- Product ID
- 55700-767_6e90a3dc-a277-4c41-a177-087cb37d63cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208644
- Marketing category
- ANDA
- Marketing start
- 2019-06-21
- Marketing end
- 0000-00-00
- Substance
- RABEPRAZOLE SODIUM
- Active strength
- 20 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 |
|---|
| 55700-767 | RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE [QUALITY CARE PRODUCTS, LLC] | 5 | Legacy NDC | 20241220_c75fab51-c34f-4be2-b6fd-382e5e89b6a4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-767-30 | 55700076730 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-767-30) | 2019-06-21 | 0000-00-00 | No | No | Current |
| 55700-767-60 | 55700076760 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-767-60) | 2019-06-21 | 0000-00-00 | No | No | Current |