Pantoprazole Sodium
- Product NDC
- 43063-618
- 11-digit product format
- 430630618
- Labeler code
- 43063
- Product ID
- 43063-618_cb6ec7ec-5ebd-f120-e053-2995a90a346c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pantoprazole Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA202038
- Marketing category
- ANDA
- Marketing start
- 2015-05-01
- Marketing end
- 2022-10-31
- Substance
- PANTOPRAZOLE SODIUM
- Active strength
- 40 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 |
|---|
| 43063-618-30 | 43063061830 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-618-30) | 2015-05-02 | 0000-00-00 | No | No | Current |