RABEPRAZOLE SODIUM
- Product NDC
- 63187-788
- 11-digit product format
- 631870788
- Labeler code
- 63187
- Product ID
- 63187-788_937ace02-fbbc-411d-9369-2b6eb02e1388
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RABEPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078964
- Marketing category
- ANDA
- Marketing start
- 2013-11-08
- 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
- 2020-12-31
- 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 |
|---|
| 63187-788 | RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE [PROFICIENT RX LP] | 2 | Legacy NDC | 20191115_59583d5a-3d1c-4407-8222-769f7290e5e6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-788-30 | 63187078830 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-30) | 2013-11-08 | 0000-00-00 | No | No | Current |
| 63187-788-60 | 63187078860 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-60) | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-788-90 | 63187078890 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-788-90) | 2013-11-08 | 0000-00-00 | No | No | Current |