NDC 61919-024
Nitrofurantion 50 mg capsule
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-232.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sidmak Laboratories (India) Private Limited | Dehradun, India | Makes it | No problems foundMay 13, 2023 · 5 inspections |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · relabels it
Recalls
- Jul 9, 2024 · Class II · Sun Pharmaceutical Industries Inc
Failed Dissolution Specifications
Lots: Lot #s: 231067, 231069, Exp 04/30/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nitrofurantoin: every company that makes it
- Form
- capsule
- Strength
- 50 mg
- Approval
- ANDA ANDA201722
- On the market since
- Apr 15, 2016
- Package NDCs
61919-024-28- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?