NDC 76420-831
Cephalexin 500 mg capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-122.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Mandideep, India | Makes it | Serious problems, FDA actionNov 23, 2022 · 6 inspections, 3 with FDA action |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Cephalexin: every company that makes it
- Form
- capsule, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA065229
- On the market since
- Sep 7, 2023
- Package NDCs
76420-831-1076420-831-3076420-831-4076420-831-42- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
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