Pantoprazole Sodium
- Product NDC
- 71335-1667
- 11-digit product format
- 713351667
- Labeler code
- 71335
- Product ID
- 71335-1667_cbd0c624-bff4-4c50-9fb0-1e99ce124119
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pantoprazole sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090970
- Marketing category
- ANDA
- Marketing start
- 2011-01-19
- Marketing end
- 0000-00-00
- Substance
- PANTOPRAZOLE 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 |
|---|
| 71335-1667-1 | 71335166701 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-1) | 2020-07-30 | 0000-00-00 | No | No | Current |
| 71335-1667-2 | 71335166702 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-2) | 2020-08-06 | 0000-00-00 | No | No | Current |
| 71335-1667-3 | 71335166703 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-3) | 2020-08-21 | 0000-00-00 | No | No | Current |
| 71335-1667-4 | 71335166704 | 56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-4) | 2020-07-30 | 0000-00-00 | No | No | Current |
| 71335-1667-5 | 71335166705 | 28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-5) | 2021-04-28 | 0000-00-00 | No | No | Current |
| 71335-1667-6 | 71335166706 | 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-6) | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1667-7 | 71335166707 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-7) | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1667-8 | 71335166708 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1667-8) | 2021-02-25 | 0000-00-00 | No | No | Current |