Rabeprazole Sodium
- Product NDC
- 60429-232
- 11-digit product format
- 604290232
- Labeler code
- 60429
- Product ID
- 60429-232_9ba48d80-0ef3-70c0-e053-2a95a90a6b99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- rabeprazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076885
- Marketing category
- ANDA
- Marketing start
- 2015-03-02
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record