Pantoprazole Sodium
- Product NDC
- 60687-585
- 11-digit product format
- 606870585
- Labeler code
- 60687
- Product ID
- 60687-585_e8baeb3d-6d9e-4d64-e053-2995a90a846f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078281
- Marketing category
- ANDA
- Marketing start
- 2021-02-02
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-585-01 | 60687058501 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-585-01) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-585-11) | 100 blister pack | 2021-02-01 | 0000-00-00 | No | No | Current |