NDC 62756-142
Metformin Hydrochloride 500 mg tablet, extended release
On the label: Sun Pharmaceutical Industries, Inc..
FDA lists this product, but its label isn't on DailyMed yet, so we can't show its factories. They usually appear within a few weeks.
Where it's made
Recalls
- May 4, 2021 · Class II · Sun Pharmaceutical Industries Inc
Presence of foreign substance: identified as activated carbon.
Lots: Lots #: JKX2749A, JKX2803A, JKX2804A, JKX2805A, JKX806A, JKX2945A,JKX2946A, JXK2947A, JKX2948A, JKX2952A, JKX2953A, JKX2954A & JKX3224A, Exp 6/2032; JKX3211A, JKX3212A, Exp 7/2023. - Mar 25, 2021 · Class III · Sun Pharmaceutical Industries Inc
Failed Moisture Limits: Out of specification for water content
Lots: Lot #JKU4639A, Exp 10/2022 - Jul 3, 2018 · Class II · Sun Pharmaceutical Industries, Inc.
Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.
Lots: Lot #: JKT0042A, Exp 1/2021 - Jan 28, 2014 · Class II · Caraco Pharmaceutical Laboratories, Ltd.
Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin found in a bottle of Metformin HCl ER
Lots: Batch JKM2433A, Mfg Date 04/2013; Exp 03/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA077336
- On the market since
- Feb 9, 2006
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