RABEPRAZOLE SODIUM
- Product NDC
- 70518-0656
- 11-digit product format
- 705180656
- Labeler code
- 70518
- Product ID
- 70518-0656_bb00942c-4e20-eccc-e053-2a95a90ac05f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RABEPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078964
- Marketing category
- ANDA
- Marketing start
- 2017-08-01
- 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
- 2022-12-31
- 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 |
|---|
| 70518-0656-0 | 70518065600 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0656-0) | 2017-08-01 | 0000-00-00 | No | No | Current |