NDC 70518-4266
Guanfacine extended-release 2 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Apotex Corp.'s NDC 60505-3928.
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 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
- Jan 27, 2025
- Package NDCs
70518-4266-070518-4266-1- Official label
- DailyMed (National Library of Medicine), updated Sep 2, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?