Rabeprazole Sodium
- Product NDC
- 42291-722
- 11-digit product format
- 422910722
- Labeler code
- 42291
- Product ID
- 42291-722_64021f1a-c753-6ed1-e053-2991aa0a29b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA090678
- Marketing category
- ANDA
- Marketing start
- 2013-12-19
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-722-10 | 42291072210 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-722-10) | 2013-12-19 | 0000-00-00 | No | No | Current |