NDC 50090-5960
Losartan Potassium and Hydrochlorothiazide 100 mg / 12.5 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions 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 |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
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
- Oct 30, 2012
- Package NDCs
50090-5960-050090-5960-150090-5960-2- Official label
- DailyMed (National Library of Medicine), updated May 6, 2024
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