NDC 67296-1739
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. 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
- RedPharm Drug, Eden Prairie, MN, 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
- Strength
- 0.4 mg
- Approval
- ANDA ANDA204645
- On the market since
- Jan 1, 2020
- Package NDCs
67296-1739-167296-1739-7- Official label
- DailyMed (National Library of Medicine), updated Aug 2, 2024
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