NDC 67296-1646
Tamsulosin Hydrochloride 0.4 mg capsule
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. 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
- RedPharm Drug, Eden Prairie, MN, United States · repackages 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
- Strength
- 0.4 mg
- Approval
- ANDA ANDA207405
- On the market since
- Jan 1, 2019
- Package NDCs
67296-1646-167296-1646-7- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2024
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