NDC 61919-952
Losartan Potassium 100 mg tablet
On the label: Direct Rx. It's repackaged from NDC 13668-115, made by Torrent Pharmaceuticals Limited (Losartan Potassium). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). 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 Direct Rx names for other drugs.
Recalls
- Apr 30, 2019 · Class II · Direct Rx
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level per manufacturer
Lots: Lot: 27AU1801 Exp. 02/28/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Losartan: every company that makes it
- Form
- tablet
- Strength
- 100 mg
- Approval
- ANDA ANDA090467
- On the market since
- Aug 21, 2019
- Package NDCs
61919-952-30- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?