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NDC 0008-0844 · HUMAN PRESCRIPTION DRUG · GRANULE, DELAYED RELEASE
| Generic name | PANTOPRAZOLE SODIUM |
|---|---|
| Labeler / Manufacturer | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. |
| Marketing category | New Drug Application (innovator) · App NDA022020 |
| Dosage form / route | GRANULE, DELAYED RELEASE · ORAL |
| Active ingredients | PANTOPRAZOLE SODIUM (40 mg/1) |
| Marketing started | 20080229 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).