Rabeprazole Sodium
- Product NDC
- 68788-7143
- 11-digit product format
- 687887143
- Labeler code
- 68788
- Product ID
- 68788-7143_5627c9c5-3a49-4ff1-8515-461231402e8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RABEPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA204237
- Marketing category
- ANDA
- Marketing start
- 2018-04-20
- 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