NDC 72189-098
Losartan Potassium And Hydrochlorothiazide 100 mg / 12.5 mg tablet, film coated
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7369.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Recalls
- May 5, 2022 · Class II · Direct Rx
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Lots: a) 30-count bottles- Lot: 11MY2103 Exp. 11/30/22 Lot: 05JA2106 Exp. 6/30/22 b) 90-count bottles- Lot: 20MY2115 Exp. 11/30/22 Lot: 22JU2118 Exp. 12/31/22 Lot: 29JY2113 Exp. 12/31/22 Lot: 13SE2113 Exp. 2/28/23 Lot: 05JA2106 Exp. 6/30/22
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 ANDA077157
- On the market since
- Jun 12, 2020
- Package NDCs
72189-098-90- Official label
- DailyMed (National Library of Medicine), updated Jan 17, 2025
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