Rabeprazole Sodium
- Product NDC
- 55700-238
- 11-digit product format
- 557000238
- Labeler code
- 55700
- Product ID
- 55700-238_939ab512-64d2-4cae-9771-24b923f02ee0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090678
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-238-30 | 55700023830 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-238-30) | 2015-04-10 | 0000-00-00 | No | No | Current |