NDC 72189-213
Alprazolam 1 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-706.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Centaur Pharmaceuticals Private Limited | Pune, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 8, 2023 · 5 inspections, 1 with FDA action |
| Centaur Pharmaceuticals Private Limited | Pernem, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyNov 14, 2025 · 1 inspection |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Recalls
- Mar 22, 2023 · Class II · Direct Rx
CGMP Deviations: Repackaging firm recalling due to potential product cross contamination concerns at the manufacturer.
Lots: Lots: a) 03FE2318, Exp. 8/31/24; b) 27FE2315, 28FE2313, 02MA2306, 21SE2201, 16NO2216, 17NO2216, 24FA2314, Exp. 8/31/24; 17FE2203, 12AP2204, 17MA2205, Exp. 3/31/23; 21JU2206, 22JU2220, 12JY2206, Exp. 5/31/23; 10AU2209, Exp. 6/30/23; 14DE2215, Exp. 9/30/24; 05JA2304, 27JA2301, Exp. 11/30/24.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Alprazolam: every company that makes it
- Form
- tablet
- Strength
- 1 mg
- Approval
- ANDA ANDA207507
- On the market since
- May 27, 2021
- Package NDCs
72189-213-3072189-213-60- Official label
- DailyMed (National Library of Medicine), updated Jun 29, 2023
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