NDC 60505-3928
Guanfacine extended-release 2 mg tablet, extended release
On the label: Apotex Corp..
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 Apotex Corp. names for other drugs.
Recalls
- Mar 31, 2021 · Class II · Apotex Corp.
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Lots: Lot #: RX1662, RX1663, RX1664 Exp. 11/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Guanfacine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 2 mg
- Approval
- ANDA ANDA205430
- On the market since
- Oct 3, 2018
- Package NDCs
60505-3928-160505-3928-360505-3928-8- Official label
- DailyMed (National Library of Medicine), updated May 6, 2026
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