RABEPRAZOLE SODIUM
- Product NDC
- 71335-0027
- 11-digit product format
- 713350027
- Labeler code
- 71335
- Product ID
- 71335-0027_6afb26af-195b-42a4-938e-f52e257a3f8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RABEPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078964
- Marketing category
- ANDA
- Marketing start
- 2013-11-08
- 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
- 2023-12-31
- 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 |
|---|
| 71335-0027-2 | 71335002702 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0027-2) | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-0027-3 | 71335002703 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0027-3) | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-0027-4 | 71335002704 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0027-4) | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-0027-5 | 71335002705 | 28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0027-5) | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-0027-6 | 71335002706 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0027-6) | 2022-05-02 | 0000-00-00 | No | No | Current |