NDC 59746-337
Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg tablet, film coated
On the label: Jubilant Cadista Pharmaceuticals Inc..
Where it's 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
- 50 mg / 12.5 mg
- Approval
- ANDA ANDA201845
- On the market since
- Oct 30, 2012
- Package NDCs
59746-337-0159746-337-1059746-337-3059746-337-90- Official label
- DailyMed (National Library of Medicine), updated Dec 5, 2025
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