NDC 76420-316
Diazepam 10 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-654.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Diazepam: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA217843
- On the market since
- Dec 14, 2023
- Package NDCs
76420-316-0076420-316-0176420-316-0576420-316-1076420-316-2076420-316-3076420-316-6076420-316-90- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2025
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