NDC 76420-665
Alprazolam 0.5 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 59762-3720.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Recalls
- Dec 17, 2014 · Class II · Neolpharma, Inc.
Subpotent Drug
Lots: Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17
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, oral
- Strength
- 0.5 mg
- Approval
- NDA authorized generic NDA018276
- On the market since
- Oct 16, 1981
- Package NDCs
76420-665-0176420-665-3076420-665-6076420-665-90- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2024
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