NDC 45865-163
Esomeprazole Magnesium 20 mg capsule, delayed release
On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-509.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Dr. Reddy's Laboratories Limited, Medchal-Malkajgiri, India · makes it and tests it
- Medsource Pharmaceuticals, Rancho Santa Margarita, CA, United States · repackages it
Recalls
- Apr 24, 2020 · Class III · Dr. Reddy's Laboratories, Inc.
Discoloration: product contains brown pellets
Lots: Lot #: C900642, Exp. 06/2020 - Feb 6, 2019 · Class III · Dr. Reddy's Laboratories, Inc.
Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown pellets.
Lots: Lot #: a) C800589, Exp 5/2019; C706058, Exp 03/2019 Lot #: b) C704873 Exp 02/2019; C800951, C800953 Exp 06/2019.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Esomeprazole: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078279
- On the market since
- Dec 10, 2015
- Package NDCs
45865-163-3045865-163-60- Official label
- DailyMed (National Library of Medicine), updated Feb 28, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?