NDC 42291-503
Losartan Potassium and Hydrochlorothiazide 100 mg / 12.5 mg tablet, film coated
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Jubilant Cadista Pharmaceuticals Inc.'s NDC 59746-338.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| The ACME Laboratories Ltd. | Dhaka, Bangladesh | Makes it | Not inspected on record |
Recalls
- Jul 11, 2014 · Class II · Jubilant Cadista Pharmaceuticals Inc.
Presence of Foreign Substance: Tablets may contain dark blemishes identified as stainless steel.
Lots: Lot #14P0292, Exp 04/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrochlorothiazide and Losartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 100 mg / 12.5 mg
- Approval
- ANDA ANDA201845
- On the market since
- Aug 31, 2022
- Package NDCs
42291-503-1042291-503-90- Official label
- DailyMed (National Library of Medicine), updated Aug 28, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?