Rabeprazole Sodium
- Product NDC
- 0093-0064
- 11-digit product format
- 000930064
- Labeler code
- 0093
- Product ID
- 0093-0064_d94ed6c8-8be9-4b7a-86f7-7fa60264429d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rabeprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076822
- Marketing category
- ANDA
- Marketing start
- 2013-11-08
- 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 |
|---|
| 0093-0064-56 | 00093006456 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-0064-56) | 2013-11-08 | 2022-01-31 | No | No | Current |