Pantoprazole 85509-1332
Product NDC
85509-1332- Manufacturer
- Phoenix Rx Llc
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 19, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA077619
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pantoprazole Sodium | 20 mg/1 |
Drug Class
Proton Pump Inhibitor [EPC]Proton Pump Inhibitors [MoA]
Packaging Options(3)
30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-3)
60 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-6)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1332-9)