NDC 24338-852
Zenzedi 7.5 mg tablet
On the label: Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals).
Where it's 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 Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) names for other drugs.
Recalls
- Jan 4, 2024 · Class I · Azurity Pharmaceuticals, Inc.
Labeling: Label Mix-up
Lots: Lot # F230169A, Exp. 06/30/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dextroamphetamine: every company that makes it
- Form
- tablet, oral
- Strength
- 7.5 mg
- Approval
- ANDA ANDA090533
- On the market since
- May 31, 2013
- Package NDCs
24338-852-03- Official label
- DailyMed (National Library of Medicine), updated Jun 13, 2025
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