NDC 71205-217
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Ascend Laboratories, LLC's NDC 67877-450.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Feb 22, 2019 · Class II · Ascend Laboratories LLC
Failed Dissolution Specifications: High Out-of-Specification dissolution results were observed during stability testing.
Lots: Lot #: 8144652, Exp Jul 2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Tamsulosin: every company that makes it
- Form
- capsule, oral
- Strength
- 0.4 mg
- Approval
- ANDA ANDA207405
- On the market since
- Aug 11, 2017
- Package NDCs
71205-217-0771205-217-1471205-217-3071205-217-6071205-217-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?