Dr. Reddy's Laboratories Limited
Medchal-Malkajgiri, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.
NDC 50436-7073
Glimepiride 2 mg tablet
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-321.
Where the pills inside were made
Dr. Reddy's Laboratories Limited
Srikakulam, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 20, 2022. 5 inspections on record.
Repackaging site
- Unit Dose Services, · repackages it
Recalls
- Jan 18, 2024 · Class III · Ongoing
Misprint on tablet
Lots: Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026 - Jan 18, 2024 · Class III · Ongoing
Misprint on tablet
Lots: Lot: T2303609; Exp. 06/2026 Lot: T2303610; Exp. 06/2026
Product details
- Generic drug
- Glimepiride: see every company that makes it
- Form
- tablet
- Strength
- 2 mg
- Approval
- ANDA ANDA077091
- On the market since
- Oct 6, 2005
- Package NDCs
50436-7073-150436-7073-3- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?