NDC 76420-315
Diazepam 5 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-653.
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
- 5 mg
- Approval
- ANDA ANDA217843
- On the market since
- Dec 14, 2023
- Package NDCs
76420-315-0076420-315-0176420-315-0576420-315-1076420-315-2076420-315-3076420-315-6076420-315-90- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2025
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