NDC 76420-654
Alprazolam 3 mg tablet, extended release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-457.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 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
- Alprazolam: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 3 mg
- Approval
- ANDA ANDA090871
- On the market since
- Jun 7, 2011
- Package NDCs
76420-654-3076420-654-6076420-654-90- Official label
- DailyMed (National Library of Medicine), updated Jan 6, 2024
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