NDC 0008-0841 – Protonix Delayed-Release
Pantoprazole Sodium 40 mg/1 · Tablet, Delayed Release · Oral
Product NDC0008-0841
Product details
- Brand name
- Protonix Delayed-Release
- Generic name
- Pantoprazole Sodium
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- NDA · NDA020987
- Marketed since
- May 1, 2000
- Listing expires
- December 31, 2027
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 40 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0008-0841-81 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0841-81) | May 1, 2000 |
Other Protonix products
- 0008-0843 Pantoprazole Sodium 20 mg/1 · Tablet, Delayed Release · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
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- 55154-4236 Pantoprazole Sodium 40 mg/10mL · Injection, Powder, For Solution · Cardinal Health 107, LLC
- 0008-0844 Pantoprazole Sodium 40 mg/1 · Granule, Delayed Release · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- 0008-0923 Pantoprazole Sodium 40 mg/10mL · Injection, Powder, For Solution · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- 0008-4001 Pantoprazole Sodium 40 mg/10mL · Injection, Powder, For Solution · Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.