NDC 70518-0386
Doxepin Hydrochloride 150 mg capsule
On the label: Remedyrepack Inc.. It's repackaged from NDC 49884-222, made by Par Health USA, LLC (Doxepin 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 Remedyrepack Inc. names for other drugs.
Product details
- Generic drug
- Doxepin: every company that makes it
- Form
- capsule
- Strength
- 150 mg
- Approval
- ANDA ANDA071669
- On the market since
- Apr 3, 2017
- Package NDCs
70518-0386-070518-0386-1- Official label
- DailyMed (National Library of Medicine), updated Jan 5, 2026
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