NDC 68071-4872
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-159.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Recalls
- Jul 17, 2019 · Class II · Macleods Pharma Usa Inc
Failed Dissolution Specifications
Lots: a) BTP803A, exp 08/2020; b) BTP802A, exp 07/2020, BTP901A, exp 12/2020; c) BTP802B, exp 07/2020
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 ANDA204645
- On the market since
- Jan 25, 2017
- Package NDCs
68071-4872-9- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?