NDC 76420-805
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-559.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA202038
- On the market since
- Sep 28, 2012
- Package NDCs
76420-805-1076420-805-3076420-805-6076420-805-90- Official label
- DailyMed (National Library of Medicine), updated May 1, 2024
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