Rabeprazole Sodium
- Product NDC
- 42291-721
- 11-digit product format
- 422910721
- Labeler code
- 42291
- Product ID
- 42291-721_d5bf9b4d-804c-6196-e053-2a95a90a55bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA076822
- Marketing category
- ANDA
- Marketing start
- 2013-12-23
- Marketing end
- 2022-01-31
- 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
- 0000-00-00
- 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 |
|---|
| 42291-721-30 | 42291072130 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-721-30) | 2013-12-23 | 0000-00-00 | No | No | Current |