NDC 42291-031
Dutasteride and Tamsulosin Hydrochloride 0.4 mg / 0.5 mg capsule
On the label: AvKARE, Inc.. It's repackaged from NDC 10370-280, made by Par Health USA, LLC (Dutasteride and Tamsulosin Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants AvKARE, Inc. names for other drugs.
Product details
- Generic drug
- Dutasteride and Tamsulosin: every company that makes it
- Form
- capsule
- Strength
- 0.4 mg / 0.5 mg
- Approval
- ANDA ANDA202509
- On the market since
- Nov 15, 2023
- Package NDCs
42291-031-30- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2026
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