PANTOPRAZOLE SODIUM
- Product NDC
- 68788-9557
- 11-digit product format
- 687889557
- Labeler code
- 68788
- Product ID
- 68788-9557_1f980162-90ec-4aae-a947-c7d121b59a40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PANTOPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA091231
- Marketing category
- ANDA
- Marketing start
- 2013-11-18
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record